Literature DB >> 22890214

Genetics: Mutations in KCND3 linked to spinocerebellar ataxias.

Ellen Bible.   

Abstract

Entities:  

Year:  2012        PMID： 22890214     DOI： 10.1038/nrneurol.2012.165

Source DB:  PubMed          Journal:  Nat Rev Neurol        ISSN： 1759-4758            Impact factor:   42.937


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  2 in total

1.  Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19.

Authors:  Anna Duarri; Justyna Jezierska; Michiel Fokkens; Michel Meijer; Helenius J Schelhaas; Wilfred F A den Dunnen; Freerk van Dijk; Corien Verschuuren-Bemelmans; Gerard Hageman; Pieter van de Vlies; Benno Küsters; Bart P van de Warrenburg; Berry Kremer; Cisca Wijmenga; Richard J Sinke; Morris A Swertz; Harm H Kampinga; Erik Boddeke; Dineke S Verbeek
Journal:  Ann Neurol       Date:  2012-12       Impact factor: 10.422

2.  Mutations in KCND3 cause spinocerebellar ataxia type 22.

Authors:  Yi-Chung Lee; Alexandra Durr; Karen Majczenko; Yen-Hua Huang; Yu-Chao Liu; Cheng-Chang Lien; Pei-Chien Tsai; Yaeko Ichikawa; Jun Goto; Marie-Lorraine Monin; Jun Z Li; Ming-Yi Chung; Emeline Mundwiller; Vikram Shakkottai; Tze-Tze Liu; Christelle Tesson; Yi-Chun Lu; Alexis Brice; Shoji Tsuji; Margit Burmeister; Giovanni Stevanin; Bing-Wen Soong
Journal:  Ann Neurol       Date:  2012-12       Impact factor: 10.422
  2 in total

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