검색결과 : 3건
| No. | Article |
|---|---|
| 1 |
A putative disease-associated haplotype within the SCN1A gene in Dravet syndrome Fendri-Kriaa N, Boujilbene S, Kammoun F, Mkaouar-Rebai E, Ben Mahmoud A, Hsairi I, Rebai A, Triki C, Fakhfakh F Biochemical and Biophysical Research Communications, 408(4), 654, 2011 |
| 2 |
Scn1a missense mutation impairs GABA(A) receptor-mediated synaptic transmission in the rat hippocampus Ohno Y, Sofue N, Ishihara S, Mashimo T, Sasa M, Serikawa T Biochemical and Biophysical Research Communications, 400(1), 117, 2010 |
| 3 |
Significant correlation of the SCN1A mutations and severe myoclonic epilepsy in infancy Ohmori I, Ouchida M, Ohtsuka Y, Oka E, Shimizu K Biochemical and Biophysical Research Communications, 295(1), 17, 2002 |