Mutations inKCND3cause spinocerebellar ataxia type 22

Molecular Dynamics Investigation of the ω-Current in the Kv1.2 Voltage Sensor Domains

(2012) Fatemeh Khalili-Araghi et al.   BIOPHYSICAL JOURNAL

Update on degenerative ataxias

(2011) Thomas Klockgether   CURRENT OPINION IN NEUROLOGY

Transient outward current (Ito) gain-of-function mutations in the KCND3-encoded Kv4.3 potassium channel and Brugada syndrome

(2011) John R. Giudicessi et al.   HEART RHYTHM

Comparison of cerebellar ataxias: A three-year prospective longitudinal assessment

(2011) Yi-chung Lee et al.   MOVEMENT DISORDERS

Frequency of KCNC3 DNA Variants as Causes of Spinocerebellar Ataxia 13 (SCA13)

(2011) Karla P. Figueroa et al.   PLoS One

Molecular Dissection of IA in Cortical Pyramidal Neurons Reveals Three Distinct Components Encoded by Kv4.2, Kv4.3, and Kv1.4  -Subunits

(2010) A. J. Norris et al.   JOURNAL OF NEUROSCIENCE

Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond

(2010) Alexandra Durr   LANCET NEUROLOGY

A map of human genome variation from population-scale sequencing

(2010) Richard M. Durbin et al.   NATURE

Molecular determinants of cardiac transient outward potassium current (Ito) expression and regulation

(2009) Noriko Niwa et al.   JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY

MPZ mutation G123S characterization: Evidence for a complex pathogenesis in CMT disease

(2008) Y. C. Lee et al.   NEUROLOGY

Novel mutation inKCNA1 causes episodic ataxia with paroxysmal dyspnea

(2007) Steven J. Shook et al.   MUSCLE & NERVE