Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Brugada Syndrome and GPD1L[original query] |
---|
Mutation analysis of the glycerol-3 phosphate dehydrogenase-1 like (GPD1L) gene in Japanese patients with Brugada syndrome. Circulation journal : official journal of the Japanese Circulation Society 2008 Oct 72 (10): 1705-6. Makiyama Takeru, Akao Masaharu, Haruna Yoshisumi, Tsuji Keiko, Doi Takahiro, Ohno Seiko, Nishio Yukiko, Kita Toru, Horie Mino |
Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome. PloS one 2015 10 (7): e0133037. Allegue Catarina, Coll Mònica, Mates Jesus, Campuzano Oscar, Iglesias Anna, Sobrino Beatriz, Brion Maria, Amigo Jorge, Carracedo Angel, Brugada Pedro, Brugada Josep, Brugada Ram |
The role of GPD1L, a sodium channel interacting gene, in the pathogenesis of Brugada Syndrome. Frontiers in medicine 2024 7 10 1159586. Alexander M Greiner, Haider Mehdi, Chloe Cevan, Rebecca Gutmann, Barry Lond |
- Page last reviewed:Feb 1, 2024
- Content source: