Retinal degeneration characterizes a spinocerebellar ataxia mapping to chromosome 3p

Nature Genetics

Volumn 10, Issue 1, 1995, Pages 89-93

  Gouw, Launce G ^a   Kaplan, Craig D ^a   Haines, John H ^b   Digre, Kathleen B ^a   Lane Rutledge, S ^c   Matilla, Antoni ^d   Leppert, Mark ^a   Zoghbi, Huda Y ^d   Ptácek, Louis J ^a  

^a UNIVERSITY OF UTAH   (United States)

^b Department of Oregon ^*  (United States)

^c UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

^d BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CEREBELLAR ATAXIA; CHROMOSOME 3P; GENE LOCATION; GENE LOCUS; GENE MAPPING; GENETIC LINKAGE; GENETIC RECOMBINATION; HUMAN; NEUROLOGIC DISEASE; PRIORITY JOURNAL; RETINA DEGENERATION; SPINOCEREBELLAR DEGENERATION; VISUAL DISORDER;

ADOLESCENT; ADULT; AGE OF ONSET; ALLELES; CAUCASOID RACE; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 3; COLOR VISION DEFECTS; FEMALE; GENETIC MARKERS; HUMAN; INFANT; INFANT, NEWBORN; LINKAGE (GENETICS); MALE; MIDDLE AGE; NEGROID RACE; PEDIGREE; RETINAL DEGENERATION; SPINOCEREBELLAR DEGENERATIONS; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0029048660     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng0595-89     Document Type: Article

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