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[Mutations in the human CACNA1A gene, encoding the pore-forming ?1 subunit of CaV2.1 (P/Q-type) calcium channels, underlie several neurological disorders, including Episodic Ataxia type 2 and Familial Hemiplegic Migraine type 1 (FHM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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