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Article

A patient with episodic ataxia and paramyotonia congenita due to mutations in KCNA1 and SCN4A.

Neurology - 22 Sept 2009

Rajakulendran S, Tan S V, Matthews E, Tomlinson S E, Labrum R, Sud R, Kullmann D M, Schorge S, Hanna M G

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 19770477
DOI: 10.1212/WNL.0b013e3181b87959
PMCID: PMC2754337

Genes

KCNA1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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A patient with episodic ataxia and paramyotonia congenita due to mutations in KCNA1 and SCN4A.PMID 19770477Read ↗

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Genetic paroxysmal neurological disorders featuring episodic ataxia and epilepsy.Semantic proximity Read ↗

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