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Article

Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4

1 Nov 1996

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 8898206
DOI: 10.1016/s0092-8674(00)81373-2

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Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4PMID 8898206Read ↗

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The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.Semantic proximity Read ↗

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