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From mice to men: TRPC3 in cerebellar ataxia

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.

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Bibliografiske detaljer
Udgivet i:Cerebellum
Hovedforfatter: Becker, Esther B. E.
Format: Artigo
Sprog:Inglês
Udgivet: 2017
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6034647/
https://ncbi.nlm.nih.gov/pubmed/25772041
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12311-015-0663-y
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