Relations between genotype and phenotype in German patients with the Machado-Joseph disease mutation.

Author:

Schols L,Amoiridis G,Epplen J T,Langkafel M,Przuntek H,Riess O

Publisher

BMJ

Subject

Psychiatry and Mental health,Clinical Neurology,Surgery

Reference41 articles.

1. Hereditary ataxia and HLA genotypes;Yakura, H.; Wakisaka, A.; Fujimoto, S.; Itakura, K.;N Engl _7 Med,1974

2. Spinocerebellar ataxia and HLA-linkage. Risk prediction by HLA typing;Jackson, J.F.; Currier, R.D.; Terasaki, P.I.; Morton, N.E.,1977

3. Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 1 2q23-24-1;Gispert, S.; Twells, R.; Orozco, G.;Nature Genet,1993

4. The gene for Machado-Joseph disease maps to human chromosome 14q;Takiyama, Y.; Nishizawa, M.; Tanaka, H.;Nature Genet,1993

5. Autosomal dominant spinocerebellar ataxia: clinical description of a distinct hereditary ataxia and genetic localization to chromosome 16 (SCA4) in a Utah kindred;Gardner, K.; Alderson, K.; Galster, B.; Kaplan, C.; Leppert, M.; Pracek, L.;Neurology,1994

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