Large, expanded repeats in SCA8 are not confined to patients with cerebellar ataxia

Nature Genetics

Volumn 24, Issue 3, 2000, Pages 214-215

  Worth, Paul F ^a   Houlden, Henry ^a   Giunti, Paola ^a   Davis, Mary B ^a   Wood, Nicholas W ^a   Moseley, Melinda L ^b,d   Schut, Lawrence J ^c   Bird, Thomas D ^e   Day, John W ^c,d   Ranum, Laura P W ^b,d  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b Genetics and Cell Development   (United States)

^c Departments of Neurology   (United Kingdom)

^d UNIVERSITY OF MINNESOTA   (United States)

^e VETERANS AFFAIRS MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ALLELE; CEREBELLAR ATAXIA; CONTROLLED STUDY; FEMALE; GENE LINKAGE DISEQUILIBRIUM; GENE MAPPING; GENETIC LINKAGE; GENETIC POLYMORPHISM; GENETIC SCREENING; GENOTYPE; HUMAN; LETTER; MAJOR CLINICAL STUDY; MALE; NUCLEOTIDE REPEAT; PRIORITY JOURNAL;

ADULT; AGED; AGED, 80 AND OVER; ALLELES; FEMALE; GENES, DOMINANT; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HEREDITARY MOTOR AND SENSORY NEUROPATHIES; HUMANS; MALE; MIDDLE AGED; NERVE TISSUE PROTEINS; PARKINSON DISEASE; PEDIGREE; PHENOTYPE; SPINOCEREBELLAR ATAXIAS; TRINUCLEOTIDE REPEATS;

ATAXIA;

EID: 0034007097     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/73411     Document Type: Letter

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