The relationship between CAG repeat length and clinical progression in Huntington's disease

Author:

Ravina Bernard,Romer Megan,Constantinescu Radu,Biglan Kevin,Brocht Alicia,Kieburtz Karl,Shoulson Ira,McDermott Michael P.

Funder

NIH

NINDS

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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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