Retinal degeneration characterizes a spinocerebellar ataxia mapping to chromosome 3p
- 1 May 1995
- journal article
- research article
- Published by Springer Nature in Nature Genetics
- Vol. 10 (1) , 89-93
- https://doi.org/10.1038/ng0595-89
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11Nature Genetics, 1994
- Autosomal dominant cerebellar ataxia with retinal degenerationNeurology, 1994
- HIV or zidovudine myopathy?Neurology, 1994
- Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23–24.1Nature Genetics, 1993
- Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1Nature Genetics, 1993
- Olivopontocerebellar Atrophy with Retinal DegenerationOphthalmology, 1993
- Autosomal dominant spinocerebellar ataxiaNeurology, 1992
- Regional mapping of the gene for autosomal dominant spinocerebellar ataxia (SCA1) by localizing the closely linked D6S89 locus to 6p24.2→p23.05Cytogenetic and Genome Research, 1992
- Spinocerebellar Ataxia and HLA LinkageNew England Journal of Medicine, 1977
- THE OLIVOPONTOCEREBELLAR ATROPHIESMedicine, 1970