검색결과 : 3건
| No. | Article |
|---|---|
| 1 |
PRRT2 Mutations Are Related to Febrile Seizures in Epileptic Patients He ZW, Qu J, Zhang Y, Mao CX, Wang ZB, Mao XY, Deng ZY, Zhou BT, Yin JY, Long HY, Xiao B, Zhang Y, Zhou HH, Liu ZQ International Journal of Molecular Sciences, 15(12), 23408, 2014 |
| 2 |
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 |
| 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 |