Familial hyperkalemic periodic paralysis caused by a de novo mutation in the sodium channel gene SCN4A.

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Molecular cloning of ion channels in Felis catus that are related to periodic paralyses in man: a contribution to the understanding of the genetic susceptibility to feline neck ventroflexion and paralysis.

P2860

Q42064066-591D364D-F38D-46F1-ABA8-835DF5A95AB2

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Familial hyperkalemic periodic paralysis caused by a de novo mutation in the sodium channel gene SCN4A.

Item

http://www.wikidata.org/entity/Q40284658

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2011 nî lūn-bûn

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2011年の論文

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2011年論文

@yue

2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

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2011年論文

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2011年论文

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2011年论文

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2011年论文

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name

Familial hyperkalemic periodic ...... the sodium channel gene SCN4A.

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type

Item

label

Familial hyperkalemic periodic ...... the sodium channel gene SCN4A.

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Familial hyperkalemic periodic ...... the sodium channel gene SCN4A.

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P1476

Familial hyperkalemic periodic ...... the sodium channel gene SCN4A.

@en

P2093

Ji-Yeon Han

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June-Bum Kim

http://www.w3.org/2001/XMLSchema#string

P2860

A1152D mutation of the Na+ channel causes paramyotonia congenita and emphasizes the role of DIII/S4-S5 linker in fast inactivation

Severe infantile hyperkalaemic periodic paralysis and paramyotonia congenita: broadening the clinical spectrum associated with the T704M mutation in SCN4A

Hyperkalemic periodic paralysis and paramyotonia congenita--a novel sodium channel mutation

Congenital myasthenic syndromes

Correlating phenotype and genotype in the periodic paralyses

Genotype-phenotype correlation and therapeutic rationale in hyperkalemic periodic paralysis

The Genotype and Clinical Phenotype of Korean Patients with Familial Hypokalemic Periodic Paralysis

Voltage-gated ion channels and hereditary disease.

An atypical phenotype of hypokalemic periodic paralysis caused by a mutation in the sodium channel gene SCN4A.

Molecular pathophysiology of voltage-gated ion channels.

P304

470-472

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P31

scholarly article

case report

P356

10.3345/KJP.2011.54.11.470

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P478

http://www.w3.org/2001/XMLSchema#string

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2011-11-30T00:00:00Z

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221755550

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P698

22253644

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P932

3254893

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Familial hyperkalemic periodic paralysis caused by a de novo mutation in the sodium channel gene SCN4A.

about

P2860

P2860

Familial hyperkalemic periodic paralysis caused by a de novo mutation in the sodium channel gene SCN4A.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P932