IndraLab

Statements

CACNA1A binds ATXN3. 3 / 3
| 1 2
sparser
"Mutations in CACNA1A are also associated with other autosomal dominant neurological disorders characterized by cerebellar dysfunction, such as EA2 (Ophoff et al. xref )."
24498617
reach
"We also analyzed the possibility of genetic interactions between ATXN1 and ATXN2, ATXN2 and ATXN3, and ATXN2 and CACNA1A."
24534762
sparser
"Several autosomal dominant human neurological disorders are associated with mutations in the CACNA1A gene including; familial hemiplegic migraine, generalized epilepsy with ataxia, episodic ataxia type 2 and spinocerebellar ataxia type-6."
20043243