PLPP2 c.53-567A>G

Variant ID: 19-288738-T-C

NM_003712.3(PLPP2):c.53-567A>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Multi-Omic analyses characterize the ceramide/sphingomyelin pathway as a therapeutic target in Alzheimer's disease.

Communications Biology
Baloni, Priyanka P; Arnold, Matthias M; Buitrago, Luna L; Nho, Kwangsik K; Moreno, Herman H; Huynh, Kevin K; Brauner, Barbara B; Louie, Gregory G; Kueider-Paisley, Alexandra A; Suhre, Karsten K; Saykin, Andrew J AJ; Ekroos, Kim K; Meikle, Peter J PJ; Hood, Leroy L; Price, Nathan D ND; , ; Doraiswamy, P Murali PM; Funk, Cory C CC; Hernández, A Iván AI; Kastenmüller, Gabi G; Baillie, Rebecca R; Han, Xianlin X; Kaddurah-Daouk, Rima R
Publication Date: 2022-10-08

Variant appearance in text: rs12982096
PubMed Link: 36209301
Variant Present in the following documents:
  • 42003_2022_4011_MOESM1_ESM.pdf
View BVdb publication page



A Chinese family with Axenfeld-Rieger syndrome: report of the clinical and genetic findings.

International Journal Of Ophthalmology
Sun, Da-Peng DP; Dai, Yun-Hai YH; Pan, Xiao-Jing XJ; Shan, Tao T; Wang, Dian-Qiang DQ; Chen, Peng P
Publication Date: 2017

Variant appearance in text: rs12982096
PubMed Link: 28730073
Variant Present in the following documents:
  • Main text
View BVdb publication page