Intrafamilial variability in Machado-Joseph disease-Reference-Cited by-同舟云学术

Intrafamilial variability in Machado-Joseph disease

Published:1996-11 Issue:6 Volume:11 Page:741-743
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Subramony S. H.,Currier R. D.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference5 articles.

1. THE CLINICAL FEATURES AND CLASSIFICATION OF THE LATE ONSET AUTOSOMAL DOMINANT CEREBELLAR ATAXIAS

2. Autosomal dominant system degeneration in Portuguese families of the Azores Islands: A new genetic disorder involving cerebellar, pyramidal, extrapyramidal and spinal cord motor functions

3. Presumed Machado-Joseph disease: four kindreds from Mississippi. In: ed. Handbook of cerebellar disease. New York: Marcel Dekker, Inc., 1993: 353-362.

4. HLA-linked spinocerebellar ataxia: a clinical and genetic study of large Italian kindreds

5. Gametic and somatic tissue–specific heterogeneity of the expanded SCA1 CAG repeat in spinocerebellar ataxia type 1

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