Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Epilepsy and Cacna1g[original query] |
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Mutational analysis of CACNA1G in idiopathic generalized epilepsy. Mutation in brief #962. Online. Human mutation 2007 May 28 (5): 524-5. Singh Baljinder, Monteil Arnaud, Bidaud Isabelle, Sugimoto Yoshihisa, Suzuki Toshimitsu, Hamano Shin-ichiro, Oguni Hirokazu, Osawa Makiko, Alonso Maria E, Delgado-Escueta Antonio V, Inoue Yushi, Yasui-Furukori Norio, Kaneko Sunao, Lory Philippe, Yamakawa Kazuhi |
Cacna1g is a genetic modifier of epilepsy caused by mutation of voltage-gated sodium channel Scn2a. Epilepsia 2016 Apr . Calhoun Jeffrey D, Hawkins Nicole A, Zachwieja Nicole J, Kearney Jennifer |
Pharmacogenetics of antiepileptic drug efficacy in childhood absence epilepsy. Annals of neurology 2017 Mar 81 (3): 444-453. Glauser Tracy A, Holland Katherine, O'Brien Valerie P, Keddache Mehdi, Martin Lisa J, Clark Peggy O, Cnaan Avital, Dlugos Dennis, Hirtz Deborah G, Shinnar Shlomo, Grabowski Gregory, |
Multi-gene panel testing in Korean patients with common genetic generalized epilepsy syndromes. PloS one 2018 13 (6): e0199321. Lee Cha Gon, Lee Jeehun, Lee Munhya |
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals. American journal of human genetics 2019 Jul . , |
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