Episodic ataxia type 2 (EA2) is an autosomal dominant disorder arising from mutations, which commonly predict heterozygous expression of Cav2. with Cav subunits. These results indicate that Cav subunits may play a prominent role in EA2 disease pathogenesis. gene, which encodes the pore-forming 12.1 subunit of Cav2.1 voltage-gated calcium channels (Ophoff et al., 1996). The… Continue reading Episodic ataxia type 2 (EA2) is an autosomal dominant disorder arising