Cognitive and affective impairments of a novel SCA/MND crossroad mutation Asidan-Reference-Cited by-同舟云学术

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Cognitive and affective impairments of a novel SCA/MND crossroad mutation Asidan

Published:2012-02-21 Issue:8 Volume:19 Page:1070-1078
ISSN:1351-5101
Container-title:European Journal of Neurology
language:en
Short-container-title:Eur J Neurol

Author:

Abe K.,Ikeda Y.,Kurata T.,Ohta Y.,Manabe Y.,Okamoto M.,Takamatsu K.,Ohta T.,Takao Y.,Shiro Y.,Shoji M.,Kamiya T.,Kobayashi H.,Koizumi A.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-1331.2012.03669.x/fullpdf

Reference64 articles.

1. Analysis of spinocerebellar ataxia type 1 (SCA1)-related CAG trinucleotide expansion in Japan;Kameya;Neurology,1995

2. A family with mild clinical manifestations of spinocerebellar ataxia type 1 (SCA1): correlation with smaller CAG repeats;Kameya;Eur J Neurol,1995

3. Analysis of CAG trinucleotide expansion associated with Machado-Joseph disease;Watanabe;J Neurol Sci,1996

4. Analysis of spinocerebellar ataxia type 2 in Gunma prefecture in Japan; CAG trinucleotide expansion and clinical characteristics;Mizushima;J Neurol Sci,1998

5. Spinocerebellar ataxia type 6: CAG trinucleotide expansion, clinical characteristics and sperm analysis;Shizuka;Eur J Neurol,1998

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