ANKK1 c.2137G>A ;(p.E713K)

Variant ID: 11-113270828-G-A

NM_178510.1(ANKK1):c.2137G>A;(p.E713K)

This variant was identified in 623 publications

View GRCh38 version.




Publications:


Functional single nucleotide polymorphisms in dopaminergic receptors D2 predict clinical response to Cariprazine.

Frontiers In Pharmacology
De Pieri, Marco M; Ferrari, Marco M; Marino, Franca F; Traber, Rafael R; Bolla, Emilio E; Cosentino, Marco M
Publication Date: 2023

Variant appearance in text: rs1800497
PubMed Link: 37229261
Variant Present in the following documents:
  • Main text
  • fphar-14-1182393.pdf
View BVdb publication page



Local genetic correlations exist among neurodegenerative and neuropsychiatric diseases.

Npj Parkinson'S Disease
Reynolds, Regina H RH; Wagen, Aaron Z AZ; Lona-Durazo, Frida F; Scholz, Sonja W SW; Shoai, Maryam M; Hardy, John J; Gagliano Taliun, Sarah A SA; Ryten, Mina M
Publication Date: 2023-04-28

Variant appearance in text: rs1800497
PubMed Link: 37117178
Variant Present in the following documents:
  • Main text
  • 41531_2023_Article_504.pdf
View BVdb publication page



No association of the dopamine D2 receptor genetic bilocus score (rs1800497/rs1799732) on food addiction and food reinforcement in Chilean adults.

Frontiers In Behavioral Neuroscience
Hidalgo Vira, Nicole N; Oyarce, Karina K; Valladares Vega, Macarena M; Goldfield, Gary S GS; Guzmán-Gutiérrez, Enrique E; Obregón, Ana M AM
Publication Date: 2023

Variant appearance in text: rs1800497
PubMed Link: 37064299
Variant Present in the following documents:
  • Main text
  • fnbeh-17-1067384.pdf
View BVdb publication page



Workflow enabling deepscale immunopeptidome, proteome, ubiquitylome, phosphoproteome, and acetylome analyses of sample-limited tissues.

Nature Communications
Abelin, Jennifer G JG; Bergstrom, Erik J EJ; Rivera, Keith D KD; Taylor, Hannah B HB; Klaeger, Susan S; Xu, Charles C; Verzani, Eva K EK; Jackson White, C C; Woldemichael, Hilina B HB; Virshup, Maya M; Olive, Meagan E ME; Maynard, Myranda M; Vartany, Stephanie A SA; Allen, Joseph D JD; Phulphagar, Kshiti K; Harry Kane, M M; Rachimi, Suzanna S; Mani, D R DR; Gillette, Michael A MA; Satpathy, Shankha S; Clauser, Karl R KR; Udeshi, Namrata D ND; Carr, Steven A SA
Publication Date: 2023-04-03

Variant appearance in text: ANKK1: E713K
PubMed Link: 37012232
Variant Present in the following documents:
  • 41467_2023_37547_MOESM12_ESM.xlsx, sheet 2
View BVdb publication page



Comprehensive proteogenomic characterization of early duodenal cancer reveals the carcinogenesis tracks of different subtypes.

Nature Communications
Li, Lingling L; Jiang, Dongxian D; Liu, Hui H; Guo, Chunmei C; Zhao, Rui R; Zhang, Qiao Q; Xu, Chen C; Qin, Zhaoyu Z; Feng, Jinwen J; Liu, Yang Y; Wang, Haixing H; Chen, Weijie W; Zhang, Xue X; Li, Bin B; Bai, Lin L; Tian, Sha S; Tan, Subei S; Yu, Zixiang Z; Chen, Lingli L; Huang, Jie J; Zhao, Jian-Yuan JY; Hou, Yingyong Y; Ding, Chen C
Publication Date: 2023-03-29

Variant appearance in text: ANKK1: E713K; rs1800497
PubMed Link: 36991000
Variant Present in the following documents:
  • 41467_2023_37221_MOESM5_ESM.xlsx, sheet 3
View BVdb publication page



The Progress and Pitfalls of Pharmacogenetics-Based Precision Medicine in Schizophrenia Spectrum Disorders: A Systematic Review and Meta-Analysis.

Journal Of Personalized Medicine
Teng, Yuxin Y; Sandhu, Amrit A; Liemburg, Edith J EJ; Naderi, Elnaz E; Alizadeh, Behrooz Z BZ
Publication Date: 2023-03-04

Variant appearance in text: rs1800497
PubMed Link: 36983653
Variant Present in the following documents:
  • Main text
  • jpm-13-00471.pdf
View BVdb publication page



Pharmacogenetics in the Treatment of Huntington's Disease: Review and Future Perspectives.

Journal Of Personalized Medicine
García-González, Xandra X; Cubo, Esther E; Simón-Vicente, Lucía L; Mariscal, Natividad N; Alcaraz, Raquel R; Aguado, Laura L; Rivadeneyra-Posadas, Jéssica J; Sanz-Solas, Antonio A; Saiz-Rodríguez, Miriam M
Publication Date: 2023-02-22

Variant appearance in text: rs1800497
PubMed Link: 36983567
Variant Present in the following documents:
  • Main text
  • jpm-13-00385.pdf
View BVdb publication page



Genome-wide association study identifies four pan-ancestry loci for suicidal ideation in the Million Veterans Program.

Plos Genetics
Ashley-Koch, Allison E AE; Kimbrel, Nathan A NA; Qin, Xue J XJ; Lindquist, Jennifer H JH; Garrett, Melanie E ME; Dennis, Michelle F MF; Hair, Lauren P LP; Huffman, Jennifer E JE; Jacobson, Daniel A DA; Madduri, Ravi K RK; Coon, Hilary H; Docherty, Anna R AR; Kang, Jooeun J; Mullins, Niamh N; Ruderfer, Douglas M DM; , ; , ; , ; Harvey, Philip D PD; McMahon, Benjamin H BH; Oslin, David W DW; Hauser, Elizabeth R ER; Hauser, Michael A MA; Beckham, Jean C JC
Publication Date: 2023-03-20

Variant appearance in text: rs1800497
PubMed Link: 36940203
Variant Present in the following documents:
  • pgen.1010623.pdf
View BVdb publication page



Associated and intermediate factors between genetic variants of the dopaminergic D2 receptor gene and harmful alcohol use in young adults.

Addiction Biology
Mattioni, Julia J; Vansteene, Clément C; Poupon, Daphnee D; Gorwood, Philip P; Ramoz, Nicolas N
Publication Date: 2023-03

Variant appearance in text: rs1800497
PubMed Link: 36825486
Variant Present in the following documents:
  • Main text
  • ADB-28-0.pdf
View BVdb publication page



Emotional dysregulation, alexithymia and neuroticism: a systematic review on the genetic basis of a subset of psychological traits.

Psychiatric Genetics
Castellini, Giovanni G; Merola, Giuseppe Pierpaolo GP; Baccaredda, Ottone Boy OB; Pecoraro, Vincenzo V; Bozza, Bernardo B; Cassioli, Emanuele E; Rossi, Eleonora E; Bessi, Valentina V; Sorbi, Sandro S; Nacmias, Benedetta B; Ricca, Valdo V
Publication Date: 2022-12-20

Variant appearance in text: rs1800497
PubMed Link: 36729042
Variant Present in the following documents:
  • Main text
  • pg-33-79.pdf
View BVdb publication page



Emotional Intelligence in Carriers of Different СОМТ, BDNF, DRD2 and HTR2A Genotypes.

Psychology In Russia : State Of The Art
Vorobyeva, Elena V EV; Kovsh, Ekaterina M EM; Kosonogov, Vladimir V VV
Publication Date: 2022

Variant appearance in text: rs1800497
PubMed Link: 36699706
Variant Present in the following documents:
  • Main text
  • pir-15-02-06.pdf
View BVdb publication page



CYP2C19-rs4986893 confers risk to major depressive disorder and bipolar disorder in the Han Chinese population whereas ABCB1-rs1045642 acts as a protective factor.

Bmc Psychiatry
Zhang, Ting T; Rao, Qingmin Q; Lin, Kangguang K; He, Yongyin Y; Cai, Jintai J; Yang, Mengxin M; Xu, Ying Y; Hou, Le L; Lin, Yulong Y; Liu, Haiying H
Publication Date: 2023-01-25

Variant appearance in text: rs1800497
PubMed Link: 36698099
Variant Present in the following documents:
  • Main text
  • 12888_2022_Article_4514.pdf
View BVdb publication page



Therapeutic and Toxic Effects of Valproic Acid Metabolites.

Metabolites
Shnayder, Natalia A NA; Grechkina, Violetta V VV; Khasanova, Aiperi K AK; Bochanova, Elena N EN; Dontceva, Evgenia A EA; Petrova, Marina M MM; Asadullin, Azat R AR; Shipulin, German A GA; Altynbekov, Kuanysh S KS; Al-Zamil, Mustafa M; Nasyrova, Regina F RF
Publication Date: 2023-01-16

Variant appearance in text: rs1800497
PubMed Link: 36677060
Variant Present in the following documents:
  • Main text
  • metabolites-13-00134.pdf
View BVdb publication page



Risk factors for eating disorders: findings from a rapid review.

Journal Of Eating Disorders
Barakat, Sarah S; McLean, Siân A SA; Bryant, Emma E; Le, Anvi A; Marks, Peta P; , ; Touyz, Stephen S; Maguire, Sarah S
Publication Date: 2023-01-17

Variant appearance in text: rs1800497
PubMed Link: 36650572
Variant Present in the following documents:
  • Main text
  • 40337_2022_Article_717.pdf
View BVdb publication page



Expanding the prostate cancer cell line repertoire with ACRJ-PC28, an AR-negative neuroendocrine cell line derived from an African-Caribbean patient.

Cancer Research Communications
Valentine, Henkel H; Aiken, William W; Morrison, Belinda B; Zhao, Ziran Z; Fowle, Holly H; Wasserman, Jason S JS; Thompson, Elon E; Chin, Warren W; Young, Mark M; Clarke, Shannique S; Gibbs, Denise D; Harrison, Sharon S; McLaughlin, Wayne W; Kwok, Tim T; Jin, Fang F; Campbell, Kerry S KS; Horvath, Anelia A; Thompson, Rory R; Lee, Norman H NH; Zhou, Yan Y; Graña, Xavier X; Ragin, Camille C; Badal, Simone S
Publication Date: 2022-11

Variant appearance in text: ANKK1: E713K; rs1800497
PubMed Link: 36643868
Variant Present in the following documents:
  • crc-22-0245-s07.xlsx, sheet 1
View BVdb publication page



Circulating messenger RNA variants as a potential biomarker for surveillance of hepatocellular carcinoma.

Frontiers In Oncology
Block, Timothy T; Zezulinski, Daniel D; Kaplan, David E DE; Lu, Jingqiao J; Zanine, Samantha S; Zhan, Tingting T; Doria, Cataldo C; Sayeed, Aejaz A
Publication Date: 2022

Variant appearance in text: rs1800497
PubMed Link: 36582804
Variant Present in the following documents:
  • Table_6.xlsx, sheet 1
View BVdb publication page



Genetic Addiction Risk and Psychological Profiling Analyses for "Preaddiction" Severity Index.

Journal Of Personalized Medicine
Blum, Kenneth K; Han, David D; Bowirrat, Abdalla A; Downs, Bernard William BW; Bagchi, Debasis D; Thanos, Panayotis K PK; Baron, David D; Braverman, Eric R ER; Dennen, Catherine A CA; Gupta, Ashim A; Elman, Igor I; Badgaiyan, Rajendra D RD; Llanos-Gomez, Luis L; Khalsa, Jag J; Barh, Debmalya D; McLaughlin, Thomas T; Gold, Mark S MS
Publication Date: 2022-10-27

Variant appearance in text: rs1800497
PubMed Link: 36579510
Variant Present in the following documents:
  • Main text
  • jpm-12-01772.pdf
View BVdb publication page



Theorizing the Role of Dopaminergic Polymorphic Risk Alleles with Intermittent Explosive Disorder (IED), Violent/Aggressive Behavior and Addiction: Justification of Genetic Addiction Risk Severity (GARS) Testing.

Journal Of Personalized Medicine
Modestino, Edward Justin EJ; Blum, Kenneth K; Dennen, Catherine A CA; Downs, B William BW; Bagchi, Debasis D; Llanos-Gomez, Luis L; Elman, Igor I; Baron, David D; Thanos, Panayotis K PK; Badgaiyan, Rajendra D RD; Braverman, Eric R ER; Gupta, Ashim A; Gold, Mark S MS; Bowirrat, Abdalla A
Publication Date: 2022-11-23

Variant appearance in text: rs1800497
PubMed Link: 36556167
Variant Present in the following documents:
  • Main text
  • jpm-12-01946.pdf
View BVdb publication page



Pharmacogenetics and Schizophrenia-Can Genomics Improve the Treatment with Second-Generation Antipsychotics?

Biomedicines
Płaza, Olga O; Gałecki, Piotr P; Orzechowska, Agata A; Gałecka, Małgorzata M; Sobolewska-Nowak, Justyna J; Szulc, Agata A
Publication Date: 2022-12-07

Variant appearance in text: rs1800497
PubMed Link: 36551925
Variant Present in the following documents:
  • Main text
  • biomedicines-10-03165.pdf
View BVdb publication page



Gene variants in eating disorders. Focus on anorexia nervosa, bulimia nervosa, and binge-eating disorder.

Journal Of Preventive Medicine And Hygiene
Donato, Kevin K; Ceccarini, Maria Rachele MR; Dhuli, Kristjana K; Bonetti, Gabriele G; Medori, Maria Chiara MC; Marceddu, Giuseppe G; Precone, Vincenza V; Xhufi, Suela S; Bushati, Marsida M; Bozo, Dhurata D; Beccari, Tommaso T; Bertelli, Matteo M
Publication Date: 2022-06

Variant appearance in text: rs1800497
PubMed Link: 36479493
Variant Present in the following documents:
  • Main text
  • jpmh-2022-02-e297.pdf
View BVdb publication page



Buprenorphine exposure levels to optimize treatment outcomes in opioid use disorder.

Frontiers In Pharmacology
Laffont, Celine M CM; Ngaimisi, Eliford E; Gopalakrishnan, Mathangi M; Ivaturi, Vijay V; Young, Malcolm M; Greenwald, Mark K MK; Heidbreder, Christian C
Publication Date: 2022

Variant appearance in text: rs1800497
PubMed Link: 36467036
Variant Present in the following documents:
  • Main text
  • fphar-13-1052113.pdf
View BVdb publication page



Factors Associated with Eating in the Absence of Hunger among Children and Adolescents: A Systematic Review.

Nutrients
Savard, Catherine C; Bégin, Stéphanie S; Gingras, Véronique V
Publication Date: 2022-11-09

Variant appearance in text: rs1800497
PubMed Link: 36432407
Variant Present in the following documents:
  • Main text
  • nutrients-14-04715.pdf
View BVdb publication page



Proposing FDA consideration for the treatment and prophylaxis of opioid and psychostimulant abuse to incorporate the induction of DNA guided dopamine homeostasis: Anti-reward deficiency restoration solution (ARDS).

Journal Of Systems And Integrative Neuroscience
Blum, Kenneth K; Giordano, John J; Baron, David D; McLaughlin, Thomas T; Badgaiyan, Rajendra D RD
Publication Date: 2020

Variant appearance in text: rs1800497
PubMed Link: 36407844
Variant Present in the following documents:
  • Main text
  • nihms-1672848.pdf
View BVdb publication page



A Missense Variant in COMT Associated with Hearing Loss among Young Adults: The National Longitudinal Study of Adolescent to Adult Health (Add Health).

Biomedicines
Li, Chuan-Ming CM; Chen, Le L; Chen, Guanjie G; Zhang, Jianhua J; Hoffman, Howard J HJ
Publication Date: 2022-10-31

Variant appearance in text: rs1800497
PubMed Link: 36359276
Variant Present in the following documents:
  • Main text
  • biomedicines-10-02756.pdf
View BVdb publication page



Should Reward Deficiency Syndrome (RDS) Be Considered an Umbrella Disorder for Mental Illness and Associated Genetic and Epigenetic Induced Dysregulation of Brain Reward Circuitry?

Journal Of Personalized Medicine
Blum, Kenneth K; Dennen, Catherine A CA; Elman, Igor I; Bowirrat, Abdalla A; Thanos, Panayotis K PK; Badgaiyan, Rajendra D RD; Downs, B William BW; Bagchi, Debasis D; Baron, David D; Braverman, Eric R ER; Gupta, Ashim A; Green, Richard R; McLaughlin, Thomas T; Barh, Debmalya D; Gold, Mark S MS
Publication Date: 2022-10-14

Variant appearance in text: rs1800497
PubMed Link: 36294858
Variant Present in the following documents:
  • Main text
  • jpm-12-01719.pdf
View BVdb publication page



Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports
Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-10-14

Variant appearance in text: rs1800497
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM13_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM15_ESM.xlsx, sheet 2
View BVdb publication page



Aldehyde dehydrogenase 2 polymorphism is associated with chemotherapy-related cognitive impairment in patients with breast cancer who receive chemotherapy.

Cancer Medicine
Yao, Senbang S; Li, Wen W; Liu, Shaochun S; Cai, Yinlian Y; Zhang, Qianqian Q; Tang, Lingxue L; Yu, Sheng S; Jing, Yanyan Y; Yin, Xiangxiang X; Cheng, Huaidong H
Publication Date: 2022-10-06

Variant appearance in text: rs1800497
PubMed Link: 36200595
Variant Present in the following documents:
  • Main text
  • CAM4-12-5209.pdf
View BVdb publication page



A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts.

Human Genome Variation
Irum, Bushra B; Kabir, Firoz F; Shoshany, Nadav N; Khan, Shahid Y SY; Rauf, Bushra B; Naeem, Muhammad Asif MA; Qaiser, Tanveer A TA; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-09-08

Variant appearance in text: rs1800497
PubMed Link: 36075891
Variant Present in the following documents:
  • 41439_2022_208_MOESM4_ESM.xlsx, sheet 2
  • 41439_2022_208_MOESM3_ESM.xlsx, sheet 2
  • 41439_2022_208_MOESM5_ESM.xlsx, sheet 2
View BVdb publication page



CYP2C8*3 and *4 define CYP2C8 phenotype: An approach with the substrate cinitapride.

Clinical And Translational Science
Campodónico, Diana María DM; Zubiaur, Pablo P; Soria-Chacartegui, Paula P; Casajús, Ana A; Villapalos-García, Gonzalo G; Navares-Gómez, Marcos M; Gómez-Fernández, Antía A; Parra-Garcés, Raúl R; Mejía-Abril, Gina G; Román, Manuel M; Martín-Vílchez, Samuel S; Ochoa, Dolores D; Abad-Santos, Francisco F
Publication Date: 2022-11

Variant appearance in text: rs1800497
PubMed Link: 36065758
Variant Present in the following documents:
  • Main text
  • CTS-15-2613.pdf
View BVdb publication page



Temporomandibular disorder in construction workers associated with ANKK1 and DRD2 genes.

Brazilian Dental Journal
Baratto, Samantha Schaffer Pugsley SSP; Meger, Michelle Nascimento MN; Camargo, Vânia V; Nolasco, Gisele Maria Correr GMC; Mattos, Natanael Henrique Ribeiro NHR; Roskamp, Liliane L; Stechman-Neto, José J; Madalena, Isabela Ribeiro IR; Küchler, Erika Calvano EC; Baratto-Filho, Flares F
Publication Date: 2022

Variant appearance in text: rs1800497
PubMed Link: 36043564
Variant Present in the following documents:
  • Main text
  • 1806-4760-bdj-33-04-12.pdf
View BVdb publication page



Genetic etiology and clinical challenges of phenylketonuria.

Human Genomics
Elhawary, Nasser A NA; AlJahdali, Imad A IA; Abumansour, Iman S IS; Elhawary, Ezzeldin N EN; Gaboon, Nagwa N; Dandini, Mohammed M; Madkhali, Abdulelah A; Alosaimi, Wafaa W; Alzahrani, Abdulmajeed A; Aljohani, Fawzia F; Melibary, Ehab M EM; Kensara, Osama A OA
Publication Date: 2022-07-19

Variant appearance in text: rs1800497
PubMed Link: 35854334
Variant Present in the following documents:
  • 40246_2022_Article_398.pdf
View BVdb publication page



Genomic, transcriptomic, and metabolomic profiles of hiPSC-derived dopamine neurons from clinically discordant brothers with identical PRKN deletions.

Npj Parkinson'S Disease
Cukier, Holly N HN; Kim, Hyunjin H; Griswold, Anthony J AJ; Codreanu, Simona G SG; Prince, Lisa M LM; Sherrod, Stacy D SD; McLean, John A JA; Dykxhoorn, Derek M DM; Ess, Kevin C KC; Hedera, Peter P; Bowman, Aaron B AB; Neely, M Diana MD
Publication Date: 2022-06-29

Variant appearance in text: ANKK1: E713K; rs1800497
PubMed Link: 35768426
Variant Present in the following documents:
  • 41531_2022_346_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Pharmacogenomic Profile of Amazonian Amerindians.

Journal Of Personalized Medicine
Rodrigues, Juliana Carla Gomes JCG; Fernandes, Marianne Rodrigues MR; Ribeiro-Dos-Santos, André Maurício AM; de Araújo, Gilderlanio Santana GS; de Souza, Sandro José SJ; Guerreiro, João Farias JF; Ribeiro-Dos-Santos, Ândrea Â; de Assumpção, Paulo Pimentel PP; Santos, Ney Pereira Carneiro Dos NPCD; Santos, Sidney S
Publication Date: 2022-06-10

Variant appearance in text: rs1800497
PubMed Link: 35743738
Variant Present in the following documents:
  • jpm-12-00952.pdf
View BVdb publication page



A bipartite graph-based expected networks approach identifies DDR genes not associated with TMB yet predictive of immune checkpoint blockade response.

Cell Reports. Medicine
Weir, William H WH; Mucha, Peter J PJ; Kim, William Y WY
Publication Date: 2022-05-17

Variant appearance in text: ANKK1: 2137G>A; Glu713Lys
PubMed Link: 35584624
Variant Present in the following documents:
  • mmc2.xlsx, sheet 4
View BVdb publication page



Dopamine DRD2 and DRD3 Polymorphisms Involvement in Nicotine Dependence in Patients with Treatment-Resistant Mental Disorders.

Journal Of Personalized Medicine
Del Casale, Antonio A; Paolini, Marco M; Gentile, Giovanna G; Borro, Marina M; Zocchi, Clarissa C; Fiaschè, Federica F; Padovano, Alessio A; Zoppi, Teodolinda T; Modesti, Martina Nicole MN; De Luca, Ottavia O; Pomes, Leda Marina LM; Brugnoli, Roberto R; Ferracuti, Stefano S; Girardi, Paolo P; Pompili, Maurizio M; Simmaco, Maurizio M
Publication Date: 2022-04-02

Variant appearance in text: rs1800497
PubMed Link: 35455685
Variant Present in the following documents:
  • Main text
  • jpm-12-00565.pdf
View BVdb publication page



Clustering of Parkinson subtypes reveals strong influence of DRD2 polymorphism and gender.

Scientific Reports
Pelzer, Esther Annegret EA; Stürmer, Sophie S; Feis, Delia-Lisa DL; Melzer, Corina C; Schwartz, Frank F; Scharge, Marcel M; Eggers, Carsten C; Tittgemeyer, Marc M; Timmermann, Lars L
Publication Date: 2022-04-11

Variant appearance in text: rs1800497
PubMed Link: 35411010
Variant Present in the following documents:
  • Main text
  • 41598_2022_Article_9657.pdf
View BVdb publication page



Association Between DRD2 and DRD4 Polymorphisms and Eating Disorders in an Italian Population.

Frontiers In Nutrition
Ceccarini, Maria Rachele MR; Fittipaldi, Simona S; Ciccacci, Cinzia C; Granese, Erika E; Centofanti, Federica F; Dalla Ragione, Laura L; Bertelli, Matteo M; Beccari, Tommaso T; Botta, Annalisa A
Publication Date: 2022

Variant appearance in text: rs1800497
PubMed Link: 35369087
Variant Present in the following documents:
  • Main text
View BVdb publication page