Otolith function in cerebellar ataxia due to mutations in the calcium channel gene CACNA1A
Associations of Variants in the CACNA1A and CACNA1C Genes With Longitudinal Blood Pressure Changes and Hypertension Incidence: The GenSalt Study
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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