Otolith function in cerebellar ataxia due to mutations in the calcium channel gene CACNA1A
A profile of alternative RNA splicing and transcript variation of CACNA1H, a human T-channel gene candidate for idiopathic generalized epilepsies
The CACNA1B R1389H variant is not associated with myoclonus-dystonia in a large European multicentric cohort
Spinocerebellar ataxia type 2: polyQ repeat variation in the CACNA1A calcium channel modifies age of onset
Episodic Ataxia Type 2 (EA2) and Spinocerebellar Ataxia Type 6 (SCA6) Due to CAG Repeat Expansion in the CACNA1A Gene on Chromosome 19p
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abbr. for calcium channel alpha subunit 1A. See hemiplegic migraine.
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