Spinocerebellar ataxia, type 3 (SCA3) is genetically identical to Machado-Joseph disease (MJD)-Reference-Cited by-同舟云学术

Spinocerebellar ataxia, type 3 (SCA3) is genetically identical to Machado-Joseph disease (MJD)

Published:1995-09 Issue:1 Volume:132 Page:71-75
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Haberhausen Gerd,Damian Maxwell S.,Leweke Frank,Müller Ulrich

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference24 articles.

1. Cerebellar ataxia, dystonia, and tremor within a family: variable phenotypes of a single genetic disorder?;Adler;Movement Disord.,1994

2. Autosomal-dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type I;Benomar;Ann. Neurol.,1994

3. Autosomal dominant system degeneration in Portuguese families of the Azores islands: a new genetic disorder involving cerebellar, pyramidal, extrapyramidal and spinal cord motor functions;Coutinho;Neurology,1978

4. Autosomal dominant spinocerebellar ataxia: clinical description of a distinct hereditary ataxia and genetic localization to chromosome 16 (SCA4) in a Utah kindred (abstract);Gardner;Neurology,1994

5. Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23–24.1;Gispert;Nat. Genet.,1993

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