An atypical phenotype of hypokalemic periodic paralysis caused by a mutation in the sodium channel gene SCN4A.
about
Normokalemic periodic paralysis is not a distinct diseaseCloning and expression of the two new variants of Nav1.5/SCN5A in rat brainGating pore currents are defects in common with two Nav1.5 mutations in patients with mixed arrhythmias and dilated cardiomyopathy.An unexpected cause of proximal myopathySkeletal muscle na channel disorders.Familial hyperkalemic periodic paralysis caused by a de novo mutation in the sodium channel gene SCN4A.The large-conductance calcium-activated potassium channel holds the key to the conundrum of familial hypokalemic periodic paralysis.N1366S mutation of human skeletal muscle sodium channel causes paramyotonia congenita.
P2860
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P2860
An atypical phenotype of hypokalemic periodic paralysis caused by a mutation in the sodium channel gene SCN4A.
description
2010 nî lūn-bûn
@nan
2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
An atypical phenotype of hypok ...... the sodium channel gene SCN4A.
@ast
An atypical phenotype of hypok ...... the sodium channel gene SCN4A.
@en
An atypical phenotype of hypok ...... the sodium channel gene SCN4A.
@nl
type
label
An atypical phenotype of hypok ...... the sodium channel gene SCN4A.
@ast
An atypical phenotype of hypok ...... the sodium channel gene SCN4A.
@en
An atypical phenotype of hypok ...... the sodium channel gene SCN4A.
@nl
prefLabel
An atypical phenotype of hypok ...... the sodium channel gene SCN4A.
@ast
An atypical phenotype of hypok ...... the sodium channel gene SCN4A.
@en
An atypical phenotype of hypok ...... the sodium channel gene SCN4A.
@nl
P2860
P1476
An atypical phenotype of hypok ...... the sodium channel gene SCN4A.
@en
P2093
June Bum Kim
Yang Hee Park
P2860
P304
P356
10.3345/KJP.2010.53.10.909
P577
2010-10-31T00:00:00Z