Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16
- 17 March 2004
- journal article
- research article
- Published by Springer Nature in neurogenetics
- Vol. 5 (2) , 109-114
- https://doi.org/10.1007/s10048-004-0175-2
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- A Genome Scan for Modifiers of Age at Onset in Huntington Disease: The HD MAPS StudyAmerican Journal of Human Genetics, 2003
- Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington diseaseAmerican Journal of Medical Genetics Part A, 2003
- A Nonsense Mutation in MSX1 Causes Witkop SyndromeAmerican Journal of Human Genetics, 2001
- A study of the Huntington's disease associated trinucleotide repeat in the Scottish population.Journal of Medical Genetics, 1993
- Expansion of the (CAG)n repeat causing Huntington's disease in 352 patients of German originHuman Molecular 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
- A dinucleotide repeat polymorphism at the D4S127 locusHuman Molecular Genetics, 1992
- The molecular genetics of embryonic pattern formation in DrosophilaNature, 1988
- Homoeotic transformations in man: Implications for the mechanism of embryonic development and for the organization of epitheliaJournal of Theoretical Biology, 1985