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The dominantly inherited cerebellar ataxias are a clinically and genetically heterogeneous group of neurodegenerative disorders. Studies using mouse models as well as recent genetic and transcriptomic human findings point to an important role for TRPC3 signaling in cerebellar ataxia.

Original publication

DOI

10.1007/s12311-015-0663-y

Type

Journal article

Journal

Cerebellum

Publication Date

14/03/2015