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Huntington's disease: How intermediate are intermediate repeat lengths?

Published:2012-09-24 Issue:14 Volume:27 Page:1714-1717
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov. Disord.

Author:

Squitieri Ferdinando,Jankovic Joseph

Funder

Italian government to Associazione Italiana Corea di Huntington-Neuromed and to IRCCS Neuromed and by Telethon

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mds.25172/fullpdf

Reference31 articles.

1. The incidence and prevalence of Huntington's disease: A systematic review and meta-analysis;Pringsheim;Mov Disord.,2012

2. Clinical Features

3. Mutational bias provides a model for the evolution of Huntington's disease and predicts a general increase in disease prevalence;Rubinsztein;Nat Genet,1994

4. DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence;Squitieri;Hum Mol Genet,1994

5. CAG expansion in the Huntington disease gene is associated with a specific and targetable predisposing haplogroup;Warby;Am J Hum Genet,2009

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