The relationship between CAG repeat length and clinical progression in Huntington's disease
Author:
Funder
NIH
NINDS
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/mds.21988/fullpdf
Reference27 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;Cell,1993
2. The likelihood of being affected with Huntington disease by a particular age, for a specific CAG size;Brinkman;Am J Hum Genet,1997
3. Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington disease;Djousse;Am J Med Genet A,2003
4. Correlations between triplet repeat expansion and clinical features in Huntington's disease;Claes;Arch Neurol,1995
5. CAG repeat size and clinical presentation in Huntington's disease;Ashizawa;Neurology,1994
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