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Mutated CACNA1A activates SCA type 6. 1 / 1
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"Different mutations of the CACNA1A genes, which encode the immunogenic alpha-1A VGCC subunit (Ca v 2.1), can produce the autosomal dominant SCA type 6, episodic ataxia type 2 (EA2) or familial hemiplegic migraine 1 (FHM1)."