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GABRA1 and STXBP1: novel genetic causes of Dravet syndrome.
Neurology. 2014 Apr 8;82(14):1245-53. doi: 10.1212/WNL.0000000000000291. Epub 2014 Mar 12.
Neurology. 2014.
PMID: 24623842
Free PMC article.
Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy.
Cossette P, Liu L, Brisebois K, Dong H, Lortie A, Vanasse M, Saint-Hilaire JM, Carmant L, Verner A, Lu WY, Wang YT, Rouleau GA.
Cossette P, et al.
Nat Genet. 2002 Jun;31(2):184-9. doi: 10.1038/ng885. Epub 2002 May 6.
Nat Genet. 2002.
PMID: 11992121
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