Mutations inKCND3cause spinocerebellar ataxia type 22-Reference-Cited by-同舟云学术

Mutations inKCND3cause spinocerebellar ataxia type 22

Published:2012-12 Issue:6 Volume:72 Page:859-869
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Lee Yi-Chung,Durr Alexandra,Majczenko Karen,Huang Yen-Hua,Liu Yu-Chao,Lien Cheng-Chang,Tsai Pei-Chien,Ichikawa Yaeko,Goto Jun,Monin Marie-Lorraine,Li Jun Z.,Chung Ming-Yi,Mundwiller Emeline,Shakkottai Vikram,Liu Tze-Tze,Tesson Christelle,Lu Yi-Chun,Brice Alexis,Tsuji Shoji,Burmeister Margit,Stevanin Giovanni,Soong Bing-Wen

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ana.23701/fullpdf

Reference39 articles.

1. Update on degenerative ataxias;Klockgether;Curr Opin Neurol,2011

2. Spinocerebellar ataxias: an update;Soong;Curr Opin Neurol,2007

3. Frequency analysis of autosomal dominant ataxias in Taiwanese patients and clinical and molecular characterization of spinocerebellar ataxia type 6;Soong;Arch Neurol,2001

4. Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond;Durr;Lancet Neurol,2010

5. A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23;Chung;Brain,2003

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