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From Mice to Men: TRPC3 in Cerebellar Ataxia.

Abstract:
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.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1007/s12311-015-0663-y

Authors


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Institution:
University of Oxford
Division:
MSD
Department:
Physiology Anatomy & Genetics
Role:
Author
Publisher:
Springer
Journal:
Cerebellum More from this journal
Publication date:
2015-03-14
DOI:
EISSN:
1473-4230
ISSN:
1473-4222
Language:
English
Pubs id:
pubs:510318
UUID:
uuid:fd501f8e-5903-4e8c-93d5-5f2e93307431
Local pid:
pubs:510318
Source identifiers:
510318
Deposit date:
2015-06-29

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