GLA c.95T>C ;(p.L32P)

Variant ID: X-100662797-A-G

NM_000169.2(GLA):c.95T>C;(p.L32P)

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Systematic cascade screening in the Danish Fabry Disease Centre: 20 years of a national single-centre experience.

Plos One
Effraimidis, Grigoris G; Rasmussen, Åse Krogh ÅK; Dunoe, Morten M; Hasholt, Lis F LF; Wibrand, Flemming F; Sorensen, Soren S SS; Lund, Allan M AM; Kober, Lars L; Bundgaard, Henning H; Yazdanfard, Puriya D W PDW; Oturai, Peter P; Larsen, Vibeke A VA; de Abreu, Vitor Hugo Fraga VHF; Enevoldsen, Lotte Hahn LH; Kristensen, Tatiana T; Svenstrup, Kirsten K; Bille, Margrethe Bastholm MB; Arif, Farah F; Mogensen, Mette M; Klokker, Mads M; Backer, Vibeke V; Kistorp, Caroline C; Feldt-Rasmussen, Ulla U
Publication Date: 2022

Variant appearance in text: GLA: L32P
PubMed Link: 36383556
Variant Present in the following documents:
  • pone.0277767.pdf
View BVdb publication page



Parkinson's disease prevalence in Fabry disease: A survey study.

Molecular Genetics And Metabolism Reports
Wise, Adina H AH; Yang, Amy A; Naik, Hetanshi H; Stauffer, Chanan C; Zeid, Natasha N; Liong, Christopher C; Balwani, Manisha M; Desnick, Robert J RJ; Alcalay, Roy N RN
Publication Date: 2018-03

Variant appearance in text: GLA: L32P
PubMed Link: 29159076
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



Oral pharmacological chaperone migalastat compared with enzyme replacement therapy in Fabry disease: 18-month results from the randomised phase III ATTRACT study.

Journal Of Medical Genetics
Hughes, Derralynn A DA; Nicholls, Kathleen K; Shankar, Suma P SP; Sunder-Plassmann, Gere G; Koeller, David D; Nedd, Khan K; Vockley, Gerard G; Hamazaki, Takashi T; Lachmann, Robin R; Ohashi, Toya T; Olivotto, Iacopo I; Sakai, Norio N; Deegan, Patrick P; Dimmock, David D; Eyskens, François F; Germain, Dominique P DP; Goker-Alpan, Ozlem O; Hachulla, Eric E; Jovanovic, Ana A; Lourenco, Charles M CM; Narita, Ichiei I; Thomas, Mark M; Wilcox, William R WR; Bichet, Daniel G DG; Schiffmann, Raphael R; Ludington, Elizabeth E; Viereck, Christopher C; Kirk, John J; Yu, Julie J; Johnson, Franklin F; Boudes, Pol P; Benjamin, Elfrida R ER; Lockhart, David J DJ; Barlow, Carrolee C; Skuban, Nina N; Castelli, Jeffrey P JP; Barth, Jay J; Feldt-Rasmussen, Ulla U
Publication Date: 2017-04

Variant appearance in text: GLA: L32P
PubMed Link: 27834756
Variant Present in the following documents:
  • Main text
  • jmedgenet-2016-104178supp001.pdf
  • jmedgenet-2016-104178.pdf
View BVdb publication page



GESPA: classifying nsSNPs to predict disease association.

Bmc Bioinformatics
Khurana, Jay K JK; Reeder, Jay E JE; Shrimpton, Antony E AE; Thakar, Juilee J
Publication Date: 2015-07-25

Variant appearance in text: GLA: L32P
PubMed Link: 26206375
Variant Present in the following documents:
  • 12859_2015_673_MOESM1_ESM.xls, sheet 2
View BVdb publication page