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Journal article

Candidate screening of the TRPC3 gene in cerebellar ataxia.

Abstract:

The hereditary cerebellar ataxias are a diverse group of neurodegenerative disorders primarily characterised by loss of balance and coordination due to dysfunction of the cerebellum and its associated pathways. Although many genetic mutations causing inherited cerebellar ataxia have been identified, a significant percentage of patients remain whose cause is unknown. The transient receptor potential (TRP) family member TRPC3 is a non-selective cation channel linked to key signalling pathways t...

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Publication status:
Published

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Publisher copy:
10.1007/s12311-011-0253-6

Authors


Becker, EB More by this author
Rajakulendran, S More by this author
Dulneva, A More by this author
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Journal:
Cerebellum (London, England)
Volume:
10
Issue:
2
Pages:
296-299
Publication date:
2011-06-05
DOI:
EISSN:
1473-4230
ISSN:
1473-4222
URN:
uuid:951b2598-6f59-4e9f-8302-793f6ee74b9e
Source identifiers:
179470
Local pid:
pubs:179470

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