Severity and Progression Rate of Cerebellar Ataxia in 16q-linked Autosomal Dominant Cerebellar Ataxia (16q-ADCA) in the Endemic Nagano Area of Japan-Reference-Cited by-同舟云学术

Severity and Progression Rate of Cerebellar Ataxia in 16q-linked Autosomal Dominant Cerebellar Ataxia (16q-ADCA) in the Endemic Nagano Area of Japan

Published:2008-10-15 Issue:1 Volume:8 Page:46-51
ISSN:1473-4222
Container-title:The Cerebellum
language:en
Short-container-title:Cerebellum

Author:

Yoshida Kunihiro,Shimizu Yusaku,Morita Hiroshi,Okano Tomomi,Sakai Haruya,Ohata Takako,Matsumoto Naomichi,Nakamura Katsuya,Tazawa Ko-ichi,Ohara Shinji,Tabata Kenichi,Inoue Atsushi,Sato Shunichi,Shimojima Yasuhiro,Hattori Takeshi,Ushiyama Masao,Ikeda Shu-ichi

Publisher

Springer Science and Business Media LLC

Subject

Clinical Neurology,Neurology

Link

http://link.springer.com/content/pdf/10.1007/s12311-008-0062-8.pdf

Reference31 articles.

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3. Takano H, Cancel G, Ikeuchi T, Lorenzetti D, Mawad R, Stevanin G et al (1998) Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations. Am J Hum Genet 63:1060–1066

4. Maruyama H, Izumi Y, Morino H, Oda M, Toji H, Nakamura S et al (2002) Difference in disease-free survival curve and regional distribution according to subtype of spinocerebellar ataxia: a study of 1,286 Japanese patients. Am J Med Genet 114:578–583

5. Sasaki H, Yabe I, Tashiro K (2003) The hereditary spinocerebellar ataxias in Japan. Cytogenet Genome Res 100:198–205

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