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[Mutations in the 1A-subunit of the brain P/Q-type calcium channel gene CACNA1A are responsible for spinocerebellar ataxia type 6 (SCA6), familial haemiplegic migraine (FHM) and episodic ataxia type 2 (EA2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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