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Article

Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1

1 Oct 1994

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 7842011
DOI: 10.1038/ng1094-136

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Related research

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Click a neighbor to travelStep 1 · 12 closest

Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1PMID 7842011Read ↗

Episodic ataxia type 1: a neuronal potassium channelopathy.Semantic proximity Read ↗

Functional characterization of a novel mutation in KCNA1 in episodic ataxia type 1 associated with epilepsy.Semantic proximity Read ↗

Primary episodic ataxias: diagnosis, pathogenesis and treatment.Semantic proximity Read ↗

A novel KCNA1 mutation in a patient with paroxysmal ataxia, myokymia, painful contractures and metabolic dysfunctionsSemantic proximity Read ↗

Three novel KCNA1 mutations in episodic ataxia type I familiesSemantic proximity Read ↗

A novel mutation in KCNA1 causes episodic ataxia without myokymiaSemantic proximity Read ↗

The episodic ataxias.Semantic proximity Read ↗

Mutations in the KCNA1 gene associated with episodic ataxia type-1 syndrome impair heteromeric voltage-gated K(+) channel function.Semantic proximity Read ↗

Clinical Spectrum of KCNA1 Mutations: New Insights into Episodic Ataxia and Epilepsy Comorbidity.Semantic proximity Read ↗

Episodic ataxia type 1 mutations in the KCNA1 gene impair the fast inactivation properties of the human potassium channels Kv1.4-1.1/Kvbeta1.1 and Kv1.4-1.1/Kvbeta1.2.Semantic proximity Read ↗

The inherited episodic ataxias: how well do we understand the disease mechanisms?Semantic proximity Read ↗

Potassium channelopathies.Semantic proximity Read ↗

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