PC c.1110C>T ;(p.N370=)

Variant ID: 11-66633733-G-A

NM_001040716.1(PC):c.1110C>T;(p.N370=)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genetic risk of Parkinson disease and progression:: An analysis of 13 longitudinal cohorts.

Neurology. Genetics
Iwaki, Hirotaka H; Blauwendraat, Cornelis C; Leonard, Hampton L HL; Liu, Ganqiang G; Maple-Grødem, Jodi J; Corvol, Jean-Christophe JC; Pihlstrøm, Lasse L; van Nimwegen, Marlies M; Hutten, Samantha J SJ; Nguyen, Khanh-Dung H KH; Rick, Jacqueline J; Eberly, Shirley S; Faghri, Faraz F; Auinger, Peggy P; Scott, Kirsten M KM; Wijeyekoon, Ruwani R; Van Deerlin, Vivianna M VM; Hernandez, Dena G DG; Day-Williams, Aaron G AG; Brice, Alexis A; Alves, Guido G; Noyce, Alastair J AJ; Tysnes, Ole-Bjørn OB; Evans, Jonathan R JR; Breen, David P DP; Estrada, Karol K; Wegel, Claire E CE; Danjou, Fabrice F; Simon, David K DK; Ravina, Bernard B; Toft, Mathias M; Heutink, Peter P; Bloem, Bastiaan R BR; Weintraub, Daniel D; Barker, Roger A RA; Williams-Gray, Caroline H CH; van de Warrenburg, Bart P BP; Van Hilten, Jacobus J JJ; Scherzer, Clemens R CR; Singleton, Andrew B AB; Nalls, Mike A MA
Publication Date: 2019-08

Variant appearance in text: PC: N370N
PubMed Link: 31404238
Variant Present in the following documents:
  • Main text
  • NG2018009605.pdf
View BVdb publication page