A novel locus for dominant cerebellar ataxia (SCA14) maps to a 10.2-cM interval flanked by D19S206 and D19S605 on chromosome 19q13.4-qter
- 1 August 2000
- journal article
- research article
- Published by Wiley in Annals of Neurology
- Vol. 48 (2) , 156-163
- https://doi.org/10.1002/1531-8249(200008)48:2<156::aid-ana4>3.0.co;2-9
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)Nature Genetics, 1999
- Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansionNature Genetics, 1997
- Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α1A-voltage-dependent calcium channelNature Genetics, 1997
- Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeatsNature Genetics, 1996
- Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECTNature Genetics, 1996
- Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2Nature Genetics, 1996
- CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1Nature Genetics, 1994
- Unstable expansion of CAG repeat in hereditary dentatorubral–pallidoluysian atrophy (DRPLA)Nature Genetics, 1994
- Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12pNature Genetics, 1994
- Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1Nature Genetics, 1993