Somatic and Germline Instability of the ATTCT Repeat in Spinocerebellar Ataxia Type 10
- 1 June 2004
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 74 (6) , 1216-1224
- https://doi.org/10.1086/421526
Abstract
No abstract availableKeywords
This publication has 37 references indexed in Scilit:
- Clinical and genetic analysis of 4 Mexican families with spinocerebellar ataxia type 10Annals of Neurology, 2001
- Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10Nature Genetics, 2000
- Mapping of a New Autosomal Dominant Spinocerebellar Ataxia to Chromosome 22American Journal of Human Genetics, 1999
- Characterization of the full fragile X syndrome mutation in fetal gametesNature Genetics, 1997
- Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α1A-voltage-dependent calcium channelNature Genetics, 1997
- Molecular analysis of juvenile Huntington disease: the major influence on (CAG)n repeat length is the sex of the affected parentHuman Molecular Genetics, 1993
- A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomesCell, 1993
- Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradoxCell, 1991
- Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndromePublished by Elsevier ,1991
- Genetic aspects of autosomal dominant late onset cerebellar ataxia.Journal of Medical Genetics, 1981