TP53 c.74+38C>T

Variant ID: 17-7579801-G-A

NM_000546.5(TP53):c.74+38C>T

This variant was identified in 57 publications

View GRCh38 version.




Publications:


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: rs1642785
PubMed Link: 36991000
Variant Present in the following documents:
  • 41467_2023_37221_MOESM5_ESM.xlsx, sheet 3
View BVdb publication page



Pharmacogenetics of chemotherapy treatment response and -toxicities in patients with osteosarcoma: a systematic review.

Bmc Cancer
Hurkmans, Evelien G E EGE; Brand, Annouk C A M ACAM; Verdonschot, Job A J JAJ; Te Loo, D Maroeska W M DMWM; Coenen, Marieke J H MJH
Publication Date: 2022-12-19

Variant appearance in text: rs1642785
PubMed Link: 36536332
Variant Present in the following documents:
  • Main text
  • 12885_2022_10434_MOESM2_ESM.pdf
  • 12885_2022_Article_10434.pdf
View BVdb publication page



Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem
Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS
Publication Date: 2022-11

Variant appearance in text: rs1642785
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



The Role of Single Nucleotide Polymorphisms in Transporter Proteins and the Folate Metabolism Pathway in Delayed Methotrexate Excretion: A Case Report and Literature Review.

Pharmacogenomics And Personalized Medicine
Wang, Jun J; Zhao, Yue-Tao YT; Sun, Meng-Jiao MJ; Chen, Feng F; Guo, Hong-Li HL
Publication Date: 2022

Variant appearance in text: rs1642785
PubMed Link: 36349164
Variant Present in the following documents:
  • Main text
  • pgpm-15-919.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: rs1642785
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM15_ESM.xlsx, sheet 2
  • 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2
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: rs1642785
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



Impact on breast cancer susceptibility and clinicopathological traits of common genetic polymorphisms in TP53, MDM2 and ATM genes in Sardinian women.

Oncology Letters
Floris, Matteo M; Pira, Giovanna G; Castiglia, Paolo P; Idda, Maria Laura ML; Steri, Maristella M; De Miglio, Maria Rosaria MR; Piana, Andrea A; Cossu, Andrea A; Azara, Antonio A; Arru, Caterina C; Deiana, Giovanna G; Putzu, Carlo C; Sanna, Valeria V; Carru, Ciriaco C; Serra, Antonello A; Bisail, Marco M; Muroni, Maria Rosaria MR
Publication Date: 2022-10

Variant appearance in text: rs1642785
PubMed Link: 36039053
Variant Present in the following documents:
  • ol-24-04-13451.pdf
View BVdb publication page



Case Report: Primary Leptomeningeal Medulloblastoma in a Child: Clinical Case Report and Literature Review.

Frontiers In Pediatrics
Morgacheva, Daria D; Daks, Alexandra A; Smirnova, Anna A; Kim, Aleksandr A; Ryzhkova, Daria D; Mitrofanova, Lubov L; Staliarova, Alena A; Omelina, Evgeniya E; Pindyurin, Alexey A; Fedorova, Olga O; Shuvalov, Oleg O; Petukhov, Alexey A; Dinikina, Yulia Y
Publication Date: 2022

Variant appearance in text: rs1642785
PubMed Link: 35899134
Variant Present in the following documents:
  • Table_1.xlsx, sheet 1
View BVdb publication page



Targeted Next-Generation Sequencing for the Identification of Genetic Predictors of Radiation-Induced Late Skin Toxicity in Breast Cancer Patients: A Preliminary Study.

Journal Of Personalized Medicine
Cargnin, Sarah S; Barizzone, Nadia N; Basagni, Chiara C; Pisani, Carla C; Ferrara, Eleonora E; Masini, Laura L; D'Alfonso, Sandra S; Krengli, Marco M; Terrazzino, Salvatore S
Publication Date: 2021-09-27

Variant appearance in text: rs1642785
PubMed Link: 34683108
Variant Present in the following documents:
  • Main text
  • jpm-11-00967.pdf
View BVdb publication page



p53/p73 Protein Network in Colorectal Cancer and Other Human Malignancies.

Cancers
Horvat, Anđela A; Tadijan, Ana A; Vlašić, Ignacija I; Slade, Neda N
Publication Date: 2021-06-09

Variant appearance in text: rs1642785
PubMed Link: 34207603
Variant Present in the following documents:
  • Main text
  • cancers-13-02885.pdf
View BVdb publication page



Identification and functional characterization of new missense SNPs in the coding region of the TP53 gene.

Cell Death And Differentiation
Doffe, Flora F; Carbonnier, Vincent V; Tissier, Manon M; Leroy, Bernard B; Martins, Isabelle I; Mattsson, Johanna S M JSM; Micke, Patrick P; Pavlova, Sarka S; Pospisilova, Sarka S; Smardova, Jana J; Joerger, Andreas C AC; Wiman, Klas G KG; Kroemer, Guido G; Soussi, Thierry T
Publication Date: 2021-05

Variant appearance in text: rs1642785
PubMed Link: 33257846
Variant Present in the following documents:
  • 41418_2020_672_MOESM3_ESM.xlsx, sheet 2
View BVdb publication page



Identification and functional characterization of new missense SNPs in the coding region of the TP53 gene.

Cell Death And Differentiation
Doffe, Flora F; Carbonnier, Vincent V; Tissier, Manon M; Leroy, Bernard B; Martins, Isabelle I; Mattsson, Johanna S M JSM; Micke, Patrick P; Pavlova, Sarka S; Pospisilova, Sarka S; Smardova, Jana J; Joerger, Andreas C AC; Wiman, Klas G KG; Kroemer, Guido G; Soussi, Thierry T
Publication Date: 2021-05

Variant appearance in text: rs1642785
PubMed Link: 33257846
Variant Present in the following documents:
  • 41418_2020_672_MOESM3_ESM.xlsx, sheet 2
View BVdb publication page



Pre- and Post-Zygotic TP53 De Novo Mutations in SHH-Medulloblastoma.

Cancers
Azzollini, Jacopo J; Schiavello, Elisabetta E; Buttarelli, Francesca Romana FR; Clerici, Carlo Alfredo CA; Tizzoni, Laura L; Vecchi, Giovanna De G; Capra, Fabio F; Pisati, Federica F; Biassoni, Veronica V; Runza, Letterio L; Carrabba, Giorgio G; Giangaspero, Felice F; Massimino, Maura M; Pensotti, Valeria V; Manoukian, Siranoush S
Publication Date: 2020-09-03

Variant appearance in text: rs1642785
PubMed Link: 32899294
Variant Present in the following documents:
  • Main text
  • cancers-12-02503.pdf
View BVdb publication page



Prevalence of germline TP53 variants among early-onset breast cancer patients from Polish population.

Breast Cancer (Tokyo, Japan)
Rogoża-Janiszewska, Emilia E; Malińska, Karolina K; Górski, Bohdan B; Scott, Rodney J RJ; Cybulski, Cezary C; Kluźniak, Wojciech W; Lener, Marcin M; Jakubowska, Anna A; Gronwald, Jacek J; Huzarski, Tomasz T; Lubiński, Jan J; Dębniak, Tadeusz T
Publication Date: 2021-01

Variant appearance in text: rs1642785
PubMed Link: 32888145
Variant Present in the following documents:
  • Main text
View BVdb publication page



Both p53 codon 72 Arg/Arg and pro/Arg genotypes in glioblastoma multiforme are associated with a better prognosis in bevacizumab treatment.

Bmc Cancer
Shen, Chiung-Chyi CC; Cheng, Wen-Yu WY; Lee, Chung-Hsin CH; Dai, Xue-Jun XJ; Chiao, Ming-Tsang MT; Liang, Yea-Jiuen YJ; Hsieh, Wan-Yu WY; Mao, Tsuo-Fei TF; Lin, Guo-Shi GS; Chen, Shou-Ren SR; Liu, Bai-Shuan BS; Chen, Jun-Peng JP
Publication Date: 2020-07-29

Variant appearance in text: rs1642785
PubMed Link: 32727419
Variant Present in the following documents:
  • Main text
  • 12885_2020_Article_7210.pdf
View BVdb publication page



Pharmacogenomics and Pharmacogenetics in Osteosarcoma: Translational Studies and Clinical Impact.

International Journal Of Molecular Sciences
Hattinger, Claudia Maria CM; Patrizio, Maria Pia MP; Luppi, Silvia S; Serra, Massimo M
Publication Date: 2020-06-30

Variant appearance in text: rs1642785
PubMed Link: 32629971
Variant Present in the following documents:
  • Main text
View BVdb publication page



TP53 p.Arg337His geographic distribution correlates with adrenocortical tumor occurrence.

Molecular Genetics & Genomic Medicine
Seidinger, Ana L AL; Caminha, Isabel P IP; Mastellaro, Maria J MJ; Gabetta, Carmen S CS; Nowill, Alexandre E AE; Pinheiro, Vitória R P VRP; Yunes, José A JA
Publication Date: 2020-09

Variant appearance in text: rs1642785
PubMed Link: 32592449
Variant Present in the following documents:
  • Main text
  • MGG3-8-e1168.pdf
View BVdb publication page



Good Cop, Bad Cop: Defining the Roles of Δ40p53 in Cancer and Aging.

Cancers
Steffens Reinhardt, Luiza L; Zhang, Xiajie X; Wawruszak, Anna A; Groen, Kira K; De Iuliis, Geoffry N GN; Avery-Kiejda, Kelly A KA
Publication Date: 2020-06-23

Variant appearance in text: rs1642785
PubMed Link: 32585821
Variant Present in the following documents:
  • Main text
View BVdb publication page



Pattern of nucleotide variants of TP53 and their correlation with the expression of p53 and its downstream proteins in a Sri Lankan cohort of breast and colorectal cancer patients.

Bmc Cancer
Manoharan, Vahinipriya V; Karunanayake, Eric Hamilton EH; Tennekoon, Kamani Hemamala KH; De Silva, Sumadee S; Imthikab, Ahamed Ilyas Ahamed AIA; De Silva, Kanishka K; Angunawela, Preethika P; Vishwakula, Sameera S; Lunec, John J
Publication Date: 2020-01-30

Variant appearance in text: rs1642785
PubMed Link: 32000721
Variant Present in the following documents:
  • Main text
  • 12885_2020_Article_6573.pdf
View BVdb publication page



The genetic association study of TP53 polymorphisms in Saudi obese patients.

Saudi Journal Of Biological Sciences
Sabir, Jamal S M JSM; El Omri, Abdelfatteh A; Shaik, Noor A NA; Banaganapalli, Babajan B; Hajrah, Nahid H NH; Zrelli, Houda H; Arfaoui, Leila L; Awan, Zuhier A ZA; Shaikh Omar, Abdulkader M AM; Mohammed, Arif A; Alharbi, Mona G MG; Alhebshi, Alawiah M AM; Jansen, Robert K RK; Khan, Muhummadh M
Publication Date: 2019-11

Variant appearance in text: rs1642785
PubMed Link: 31762593
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



Distinctive mutational spectrum and karyotype disruption in long-term cisplatin-treated urothelial carcinoma cell lines.

Scientific Reports
Skowron, Margaretha A MA; Petzsch, Patrick P; Hardt, Karin K; Wagner, Nicholas N; Beier, Manfred M; Stepanow, Stefanie S; Drechsler, Matthias M; Rieder, Harald H; Köhrer, Karl K; Niegisch, Günter G; Hoffmann, Michèle J MJ; Schulz, Wolfgang A WA
Publication Date: 2019-10-09

Variant appearance in text: rs1642785
PubMed Link: 31597922
Variant Present in the following documents:
  • 41598_2019_50891_MOESM12_ESM.xlsx, sheet 2
  • 41598_2019_50891_MOESM4_ESM.xlsx, sheet 3
  • 41598_2019_50891_MOESM8_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM2_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM3_ESM.xlsx, sheet 2
  • 41598_2019_50891_MOESM9_ESM.xlsx, sheet 3
  • 41598_2019_50891_MOESM7_ESM.xlsx, sheet 3
  • 41598_2019_50891_MOESM4_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM12_ESM.xlsx, sheet 3
  • 41598_2019_50891_MOESM5_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM8_ESM.xlsx, sheet 2
  • 41598_2019_50891_MOESM2_ESM.xlsx, sheet 2
  • 41598_2019_50891_MOESM5_ESM.xlsx, sheet 2
  • 41598_2019_50891_MOESM4_ESM.xlsx, sheet 2
  • 41598_2019_50891_MOESM5_ESM.xlsx, sheet 3
  • 41598_2019_50891_MOESM8_ESM.xlsx, sheet 3
  • 41598_2019_50891_MOESM12_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM9_ESM.xlsx, sheet 2
  • 41598_2019_50891_MOESM7_ESM.xlsx, sheet 2
  • 41598_2019_50891_MOESM3_ESM.xlsx, sheet 3
  • 41598_2019_50891_MOESM7_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM3_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM9_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM2_ESM.xlsx, sheet 3
View BVdb publication page



Intraventricular meningiomas frequently harbor NF2 mutations but lack common genetic alterations in TRAF7, AKT1, SMO, KLF4, PIK3CA, and TERT.

Acta Neuropathologica Communications
Jungwirth, Gerhard G; Warta, Rolf R; Beynon, Christopher C; Sahm, Felix F; von Deimling, Andreas A; Unterberg, Andreas A; Herold-Mende, Christel C; Jungk, Christine C
Publication Date: 2019-08-30

Variant appearance in text: rs1642785
PubMed Link: 31470906
Variant Present in the following documents:
  • 40478_2019_793_MOESM1_ESM.xlsx, sheet 2
View BVdb publication page



Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases.

Cell Death & Disease
Grassi, Ludovica L; Alfonsi, Romina R; Francescangeli, Federica F; Signore, Michele M; De Angelis, Maria Laura ML; Addario, Antonio A; Costantini, Manuela M; Flex, Elisabetta E; Ciolfi, Andrea A; Pizzi, Simone S; Bruselles, Alessandro A; Pallocca, Matteo M; Simone, Giuseppe G; Haoui, Mustapha M; Falchi, Mario M; Milella, Michele M; Sentinelli, Steno S; Di Matteo, Paola P; Stellacci, Emilia E; Gallucci, Michele M; Muto, Giovanni G; Tartaglia, Marco M; De Maria, Ruggero R; Bonci, Désirée D
Publication Date: 2019-02-27

Variant appearance in text: rs1642785
PubMed Link: 30814510
Variant Present in the following documents:
  • 41419_2019_1453_MOESM27_ESM.xlsx, sheet 2
  • 41419_2019_1453_MOESM27_ESM.xlsx, sheet 1
  • 41419_2019_1453_MOESM27_ESM.xlsx, sheet 3
View BVdb publication page



Germline TP53 mutation spectrum in Sudanese premenopausal breast cancer patients: correlations with reproductive factors.

Breast Cancer Research And Treatment
Aceto, Gitana Maria GM; Awadelkarim, Khalid Dafaallah KD; Di Nicola, Marta M; Moscatello, Carmelo C; Pantalone, Mattia Russel MR; Verginelli, Fabio F; Elwali, Nasr Eldin NE; Mariani-Costantini, Renato R
Publication Date: 2019-06

Variant appearance in text: rs1642785
PubMed Link: 30796655
Variant Present in the following documents:
  • Main text
  • 10549_2019_Article_5168.pdf
View BVdb publication page



Specific V-ATPase expression sub-classifies IDHwt lower-grade gliomas and impacts glioma growth in vivo.

Ebiomedicine
Terrasi, Andrea A; Bertolini, Irene I; Martelli, Cristina C; Gaudioso, Gabriella G; Di Cristofori, Andrea A; Storaci, Alessandra Maria AM; Formica, Miriam M; Bosari, Silvano S; Caroli, Manuela M; Ottobrini, Luisa L; Vaccari, Thomas T; Vaira, Valentina V
Publication Date: 2019-03

Variant appearance in text: rs1642785
PubMed Link: 30737087
Variant Present in the following documents:
  • mmc1.xlsx, sheet 9
View BVdb publication page



Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs1642785
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Systematic evaluation of isoform function in literature reports of alternative splicing.

Bmc Genomics
Bhuiyan, Shamsuddin A SA; Ly, Sophia S; Phan, Minh M; Huntington, Brandon B; Hogan, Ellie E; Liu, Chao Chun CC; Liu, James J; Pavlidis, Paul P
Publication Date: 2018-08-28

Variant appearance in text: rs1642785
PubMed Link: 30153812
Variant Present in the following documents:
  • 12864_2018_5013_MOESM1_ESM.pdf
View BVdb publication page



A likely pathogenic variant putatively affecting splicing of PIGA identified in a multiple congenital anomalies hypotonia-seizures syndrome 2 (MCAHS2) family pedigree via whole-exome sequencing.

Molecular Genetics & Genomic Medicine
Yang, Junli J; Wang, Qiong Q; Zhuo, Qingcui Q; Tian, Huiling H; Li, Wen W; Luo, Fang F; Zhang, Jinghui J; Bi, Dan D; Peng, Jing J; Zhou, Dong D; Xin, Huawei H
Publication Date: 2018-09

Variant appearance in text: rs1642785
PubMed Link: 29974678
Variant Present in the following documents:
  • MGG3-6-739-s002.xlsx, sheet 6
  • MGG3-6-739-s002.xlsx, sheet 5
  • MGG3-6-739-s002.xlsx, sheet 7
  • MGG3-6-739-s002.xlsx, sheet 4
View BVdb publication page



Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.

Oncotarget
Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH
Publication Date: 2017-11-10

Variant appearance in text: rs1642785
PubMed Link: 29221171
Variant Present in the following documents:
  • oncotarget-08-95841-s002.xlsx, sheet 4
View BVdb publication page



Genetic predisposition to lung cancer: comprehensive literature integration, meta-analysis, and multiple evidence assessment of candidate-gene association studies.

Scientific Reports
Wang, Junjun J; Liu, Qingyun Q; Yuan, Shuai S; Xie, Weijia W; Liu, Yuan Y; Xiang, Ying Y; Wu, Na N; Wu, Long L; Ma, Xiangyu X; Cai, Tongjian T; Zhang, Yao Y; Sun, Zhifu Z; Li, Yafei Y
Publication Date: 2017-08-21

Variant appearance in text: rs1642785
PubMed Link: 28827732
Variant Present in the following documents:
  • 41598_2017_7737_MOESM1_ESM.pdf
View BVdb publication page



Unique Features of Germline Variation in Five Egyptian Familial Breast Cancer Families Revealed by Exome Sequencing.

Plos One
Kim, Yeong C YC; Soliman, Amr S AS; Cui, Jian J; Ramadan, Mohamed M; Hablas, Ahmed A; Abouelhoda, Mohamed M; Hussien, Nehal N; Ahmed, Ola O; Zekri, Abdel-Rahman Nabawy AN; Seifeldin, Ibrahim A IA; Wang, San Ming SM
Publication Date: 2017

Variant appearance in text: rs1642785
PubMed Link: 28076423
Variant Present in the following documents:
  • pone.0167581.s001.xlsx, sheet 1
View BVdb publication page



Targeted exome sequencing reveals distinct pathogenic variants in Iranians with colorectal cancer.

Oncotarget
Ashktorab, Hassan H; Mokarram, Pooneh P; Azimi, Hamed H; Olumi, Hasti H; Varma, Sudhir S; Nickerson, Michael L ML; Brim, Hassan H
Publication Date: 2017-01-31

Variant appearance in text: rs1642785
PubMed Link: 28002797
Variant Present in the following documents:
  • oncotarget-08-7852-s002.xlsx, sheet 1
  • oncotarget-08-7852-s002.xlsx, sheet 2
View BVdb publication page



TP53 Polymorphisms and Colorectal Cancer Risk in Patients with Lynch Syndrome in Taiwan: A Retrospective Cohort Study.

Plos One
Kamiza, Abram Bunya AB; Hsieh, Ling-Ling LL; Tang, Reiping R; Chien, Huei-Tzu HT; Lai, Chih-Hsiung CH; Chiu, Li-Ling LL; Lo, Tsai-Ping TP; Hung, Kuan-Yi KY; You, Jeng-Fu JF; Wang, Wen-Chang WC; Hsiung, Chao A CA; Yeh, Chih-Ching CC
Publication Date: 2016

Variant appearance in text: rs1642785
PubMed Link: 27907203
Variant Present in the following documents:
  • Main text
  • pone.0167354.pdf
View BVdb publication page



Pharmacogenetics Biomarkers and Their Specific Role in Neoadjuvant Chemoradiotherapy Treatments: An Exploratory Study on Rectal Cancer Patients.

International Journal Of Molecular Sciences
Dreussi, Eva E; Cecchin, Erika E; Polesel, Jerry J; Canzonieri, Vincenzo V; Agostini, Marco M; Boso, Caterina C; Belluco, Claudio C; Buonadonna, Angela A; Lonardi, Sara S; Bergamo, Francesca F; Gagno, Sara S; De Mattia, Elena E; Pucciarelli, Salvatore S; De Paoli, Antonino A; Toffoli, Giuseppe G
Publication Date: 2016-09-05

Variant appearance in text: rs1642785
PubMed Link: 27608007
Variant Present in the following documents:
  • Main text
View BVdb publication page