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

The Moonwalker Mouse: New Insights into TRPC3 Function, Cerebellar Development, and Ataxia

(2014) Esther B. E. Becker   CEREBELLUM

Exome Sequencing in the Clinical Diagnosis of Sporadic or Familial Cerebellar Ataxia

(2014) Brent L. Fogel et al.   JAMA Neurology

Multigeneration family with short stature, developmental delay, and dysmorphic features due to 4q27-q28.1 microdeletion

(2013) Scott E. Hickey et al.   European Journal of Medical Genetics

Early Onset of Ataxia in Moonwalker Mice Is Accompanied by Complete Ablation of Type II Unipolar Brush Cells and Purkinje Cell Dysfunction

(2013) G. Sekerkova et al.   JOURNAL OF NEUROSCIENCE

Structure of the TRPV1 ion channel determined by electron cryo-microscopy

(2013) Maofu Liao et al.   NATURE

Clinical Neurogenetics

(2013) Vikram G. Shakkottai et al.   NEUROLOGIC CLINICS

Candidate Screening of the TRPC3 Gene in Cerebellar Ataxia

(2011) Esther B. E. Becker et al.   CEREBELLUM

A point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker mice

(2009) E. B. E. Becker et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA