
IndraLab
Statements
CACNA1A inhibits pyraclofos. 2 / 2
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"Episodic Ataxia type 2 (EA2) is the most frequent subtype of episodic ataxia caused by loss-of- function mutations in the CACNA1A gene encoding the alpha1A subunit of P/Q type voltage gated Ca 2+ channels (Ca v 2.1) mainly expressed in Purkinje and granule cells in the cerebellum."