Huntington CAG repeat size does not modify onset age in familial Parkinson's disease: TheGenePD study
- 22 July 2008
- journal article
- research article
- Published by Wiley in Movement Disorders
- Vol. 23 (11) , 1596-1601
- https://doi.org/10.1002/mds.22186
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- Selective defect of in vivo glycolysis in early Huntington's disease striatumProceedings of the National Academy of Sciences, 2007
- Huntingtin inhibits caspase-3 activationThe EMBO Journal, 2006
- The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson's disease in European populationsJournal of Medical Genetics, 2005
- HD CAG repeat implicates a dominant property of huntingtin in mitochondrial energy metabolismHuman Molecular Genetics, 2005
- Cloning of the Gene Containing Mutations that Cause PARK8-Linked Parkinson's DiseaseNeuron, 2004
- Huntington’s disease geneticsNeuroRX, 2004
- Early mitochondrial calcium defects in Huntington's disease are a direct effect of polyglutaminesNature Neuroscience, 2002
- Mutation in the α-Synuclein Gene Identified in Families with Parkinson's DiseaseScience, 1997
- 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