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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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Dades bibliogràfiques
Publicat a:Cerebellum
Autor principal: Becker, Esther B. E.
Format: Artigo
Idioma:Inglês
Publicat: 2017
Matèries:
Accés en línia: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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