Spinocerebellar ataxia type 3 phenotypically resembling Parkinson disease in a black family

Archives of Neurology

Volumn 58, Issue 2, 2001, Pages 296-299

  Gwinn Hardy, K ^a   Singleton, A ^a   O'Suilleabhain, P ^a   Boss, M ^a   Nicholl, D ^a   Adam, A ^a   Hussey, J ^a   Critchley, P ^a   Hardy, J ^a   Farrer, M ^a  

^a MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AFRICA; ANTERIOR HORN CELL; ARTICLE; FAMILY STUDY; GENE LOCUS; GENETIC LINKAGE; GENOTYPE; HUMAN; MACHADO JOSEPH DISEASE; NEGRO; PARKINSON DISEASE; PARKINSONISM; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PYRAMIDAL TRACT; SPINOCEREBELLAR DEGENERATION;

EID: 0035118860     PISSN: 00039942     EISSN: None     Source Type: Journal    
DOI: 10.1001/archneur.58.2.296     Document Type: Article

References (7)

1. Azorean disease of the nervous system
2. Dopa-responsive parkinsonism phenotype of Machado-Joseph disease: Confirmation of 14q CAG expansion
3. Joseph disease: An autosomal dominant motor system degeneration
4. Intrafamilial variability in Machado-Joseph disease
5. Joseph disease: A multisystem degenerative disorder of the nervous system
6. Correlation between CAG repeat length and clinical features in Machado-Joseph disease
7. Molecular features of the CAG repeats and clinical manifestation of Machado-Joseph disease