De novo expansion of a CAG repeat in a Japanese patient with sporadic Huntington’s disease

Author:

Watanabe Masahiko,Satoh Akiko,Kanemoto Mizuki,Ohkoshi Norio,Shoji Shin’ichi

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference17 articles.

1. The Huntington’s Disease Collaborative Research Group. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington’s disease chromosomes. Cell 1993;72:971–83.

2. A worldwide study of the Huntington’s disease mutation. The sensitivity and specificity of measuring CAG repeats;Kremer;N Eng J Med,1994

3. Population genetics study of Huntington’s chorea in Japan;Kishimoto;Annu Rep Res Inst Environ Med,1957

4. Kanazawa I. On the prevalence rate of Huntington’s disease in Ibaraki prefecture. Annual Report of the Research Committee of CNS Degenerative Diseases 1982. The Ministry of Health and Welfare of Japan, 1983, pp. 151–6.

5. Human genetics. problems and approaches;Vogel,1986

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