4p16.3 haplotype modifying age at onset of Huntington disease
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2008.01136.x/fullpdf
Reference39 articles.
1. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington’s disease chromosomes. The Huntington’s Disease Collaborative Research Group;Huntington Disease Collaborative Group;Cell,1993
2. The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington’s disease;Andrew;Nat Genet,1993
3. Correlation between the onset age of Huntington’s disease and length of the trinucleotide repeat in IT-15;Stine;Hum Mol Genet,1993
4. Instability of CAG repeats in Huntington’s disease: relation to parental transmission and age of onset;Trottier;J Med Genet,1994
5. Family and molecular data for a fine analysis of age at onset in Huntington disease;Squitieri;Am J Med Genet,2000
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2. A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomes;EBioMedicine;2019-10
3. CAG Repeat Not Polyglutamine Length Determines Timing of Huntington’s Disease Onset;Cell;2019-08
4. Huntington’s disease onset is determined by length of uninterrupted CAG, not encoded polyglutamine, and is modified by DNA maintenance mechanisms;2019-01-24
5. Risk factors for the onset and progression of Huntington disease;NeuroToxicology;2017-07
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