Mutation size and age at onset in Huntington's disease.
Open Access
- 1 December 1993
- journal article
- Published by BMJ in Journal of Medical Genetics
- Vol. 30 (12) , 1008-1011
- https://doi.org/10.1136/jmg.30.12.1008
Abstract
The mutation responsible for Huntington's disease is a polymorphic (CAG)n repeat sequence which is expanded on affected chromosomes. The number of repeat units observed on 229 affected chromosomes varied from 27 to 102, while the control chromosomes showed a range of 7 to 34 repeats. There was a highly significant relationship between the size of the expanded region and age at onset, larger mutations being associated with earlier onset. This association was strongest in those with onset before 25 years of age but less clear cut with later onset, and is therefore unlikely to be useful for predicting age at onset in the context of presymptomatic testing.Keywords
This publication has 6 references indexed in Scilit:
- Trinucleotide repeat length instability and age of onset in Huntington's diseaseNature Genetics, 1993
- Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's diseaseNature Genetics, 1993
- A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomesCell, 1993
- Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family memberPublished by Elsevier ,1992
- 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
- The natural history of Huntington disease: Possible role of “aging genes”American Journal of Medical Genetics, 1984