Do mutations in the murine ataxia gene TRPC3 cause cerebellar ataxia in humans? Journal Article


Authors: Fogel, B. L.; Hanson, S. M.; Becker, E. B. E.
Article Title: Do mutations in the murine ataxia gene TRPC3 cause cerebellar ataxia in humans?
Keywords: adult; gene mutation; gene sequence; case report; nonhuman; nuclear magnetic resonance imaging; letter; protein function; genetic variability; gene frequency; heterozygote; wild type; electromyography; transcription factor nfat; nerve cell necrosis; cerebellum vermis; brain atrophy; cerebellar ataxia; channel gating; nerve conduction; electromyogram; exome; human; male; priority journal; vanilloid receptor 1; ataxic gait; transient receptor potential channel 3
Journal Title: Movement Disorders
Volume: 30
Issue: 2
ISSN: 0885-3185
Publisher: Wiley Blackwell  
Date Published: 2015-02-01
Start Page: 284
End Page: 286
Language: English
DOI: 10.1002/mds.26096
PROVIDER: scopus
PMCID: PMC4318721
PUBMED: 25477146
DOI/URL:
Notes: Export Date: 2 March 2015 -- Source: Scopus
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  1. Sonya Merritt Hanson
    11 Hanson