Multiplex families with epilepsy: Success of clinical and molecular genetic characterization.
about
Myoclonus epilepsy and ataxia due to KCNC1 mutation: Analysis of 20 cases and K+ channel properties.Phenotypic analysis of 303 multiplex families with common epilepsies.A novel mutation in LAMC3 associated with generalized polymicrogyria of the cortex and epilepsy.Potassium Channel Gain of Function in Epilepsy: An Unresolved Paradox.Rare gene deletions in genetic generalized and Rolandic epilepsies
P2860
Multiplex families with epilepsy: Success of clinical and molecular genetic characterization.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Multiplex families with epilep ...... ular genetic characterization.
@ast
Multiplex families with epilep ...... ular genetic characterization.
@en
type
label
Multiplex families with epilep ...... ular genetic characterization.
@ast
Multiplex families with epilep ...... ular genetic characterization.
@en
prefLabel
Multiplex families with epilep ...... ular genetic characterization.
@ast
Multiplex families with epilep ...... ular genetic characterization.
@en
P2093
P2860
P50
P1433
P1476
Multiplex families with epilep ...... ular genetic characterization.
@en
P2093
Adel J Misk
Aziz Mazarib
Bruria Ben-Zeev
Dana Ekstein
Esther Kahana
Gemma L Carvill
Graeme D Jackson
Hadassa Goldberg-Stern
Heather C Mefford
Ilan Blatt
P2860
P304
P356
10.1212/WNL.0000000000002404
P407
P50
P577
2016-01-22T00:00:00Z