Do mutations in the murine ataxia geneTRPC3cause cerebellar ataxia in humans?-Reference-Cited by-同舟云学术

Do mutations in the murine ataxia geneTRPC3cause cerebellar ataxia in humans?

Published:2014-12-05 Issue:2 Volume:30 Page:284-286
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Fogel Brent L.¹,Hanson Sonya M.²³,Becker Esther B. E.⁴

Affiliation:

1. Program in Neurogenetics; Department of Neurology David Geffen School of Medicine; University of California Los Angeles; Los Angeles California USA

2. Structural Bioinformatics and Computational Biochemistry Unit; Department of Biochemistry; University of Oxford; South Parks Road Oxford OX1 3QU United Kingdom

3. Computational Biology Program; Memorial Sloan Kettering Cancer Center; New York New York 10065 USA

4. MRC Functional Genomics Unit; Department of Physiology; Anatomy and Genetics; University of Oxford; South Parks Road Oxford OX1 3PT United Kingdom

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference9 articles.

1. Clinical neurogenetics: autosomal dominant spinocerebellar ataxia;Shakkottai;Neurol Clin,2013

2. Exome sequencing in the clinical diagnosis of sporadic or familial cerebellar ataxia;Fogel;JAMA Neurol,2014

3. The moonwalker mouse: new insights into TRPC3 function, cerebellar development, and ataxia;Becker;Cerebellum,2014

4. An introduction to TRP channels;Ramsey;Annu Rev Physiol,2006

5. Structure of the TRPV1 ion channel determined by electron cryo-microscopy;Liao;Nature,2013

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