The role of the CACNA1A gene in the pathogenesis of episodic ataxia 2 and spinocerebellar ataxia 6
CACNA1A encodes for the voltage-gated calcium channel CaV2.1. Mutations to CACNA1A are known to cause an assortment of disorders, including episodic ataxia 2, spinocerebellar ataxia 6, familial hemiplegic migraine 1, and more. The pathogenic nature behind these mutations is still unknown, but recent...
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Language: | en_US |
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2021
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Online Access: | https://hdl.handle.net/2144/43357 |