SCA8 Repeat Expansion: Large CTA/CTG Repeat Alleles Are More Common in Ataxic Patients, Including Those with SCA6-Reference-Cited by-同舟云学术

SCA8 Repeat Expansion: Large CTA/CTG Repeat Alleles Are More Common in Ataxic Patients, Including Those with SCA6

Published:2003-03 Issue:3 Volume:72 Page:704-709
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Izumi Yuishin,Maruyama Hirofumi,Oda Masaya,Morino Hiroyuki,Okada Takayuki,Ito Hidefumi,Sasaki Iwao,Tanaka Hiroyasu,Komure Osamu,Udaka Fukashi,Nakamura Shigenobu,Kawakami Hideshi

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference21 articles.

1. Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in Italy;Cellini;Arch Neurol,2001

2. Loss of muscle-specific chloride channel in type 1 myotonic dystrophy due to misregulated alternative splicing;Charlet-B;Mol Cell,2002

3. Spinocerebellar ataxia type 8: clinical features in a large family;Day;Neurology,2000

4. A familial case of spinocerebellar ataxia type 8 (SCA8);Hokezu;Rinsho Shinkeigaku,2000

5. Molecular and clinical analyses of spinocerebellar ataxia type 8 in Japan;Ikeda;Neurology,2000

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