Evaluation of SCN8A as a candidate gene for autosomal dominant essential tremor.
about
De novo gain-of-function and loss-of-function mutations of SCN8A in patients with intellectual disabilities and epilepsyAnalysis of the mouse mutant Cloth-ears shows a role for the voltage-gated sodium channel Scn8a in peripheral neural hearing loss.Sodium channel SCN8A (Nav1.6): properties and de novo mutations in epileptic encephalopathy and intellectual disability.Inherited neuronal ion channelopathies: new windows on complex neurological diseases.Update on genetics of essential tremor.Recurrent and Non-Recurrent Mutations of SCN8A in Epileptic Encephalopathy.Linking Essential Tremor to the Cerebellum-Animal Model Evidence.
P2860
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P2860
Evaluation of SCN8A as a candidate gene for autosomal dominant essential tremor.
description
2008 nî lūn-bûn
@nan
2008 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Evaluation of SCN8A as a candidate gene for autosomal dominant essential tremor.
@ast
Evaluation of SCN8A as a candidate gene for autosomal dominant essential tremor.
@en
type
label
Evaluation of SCN8A as a candidate gene for autosomal dominant essential tremor.
@ast
Evaluation of SCN8A as a candidate gene for autosomal dominant essential tremor.
@en
prefLabel
Evaluation of SCN8A as a candidate gene for autosomal dominant essential tremor.
@ast
Evaluation of SCN8A as a candidate gene for autosomal dominant essential tremor.
@en
P2093
P2860
P1476
Evaluation of SCN8A as a candidate gene for autosomal dominant essential tremor.
@en
P2093
Julie M Jones
Lisa M Sharkey
Miriam H Meisler
Peter Hedera
P2860
P304
P356
10.1016/J.PARKRELDIS.2008.06.010
P577
2008-08-20T00:00:00Z