Machado-Joseph disease mutations as the genetic basis of most spinocerebellar ataxias in Germany.

Author:

Schols L,Amoiridis G,Langkafel M,Buttner T,Przuntek H,Riess O,Vieira-Saecker A M,Epplen J T

Publisher

BMJ

Subject

Psychiatry and Mental health,Clinical Neurology,Surgery

Reference11 articles.

1. Machado-Joseph disease: an autosomal dominant motor system degeneration;Rosenberg, R.N.;Mov Disord,1992

2. CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32 1;Kawaguchi, Y.; Okamoto, T.; Taniwaki, M.;Nature Genetics,1994

3. A third locus for autosomal dominant cerebellar ataxia type 1 maps to chromosome 14qqter: evidence for the existence of a fourth locus;Stevanin, G.; Le Guem, E.; Ravise, N.;Am J Humn Genet,1994

4. Machado-Joseph disease in New England: clinical description and distinction from the olivopontocerebellar atrophies;Sudarsky, L.; Corwin, L.; Dawson, D.M.;Mov Disord,1992

5. A large family with Machado-Joseph disease: clinical and genetic studies;Takiyama, Y.; Ikemoto, S.; Tanaka, Y.;Acta Neurol Scand,1989

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