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Neurology. 2013 Sep 17;81(12):1099-100. doi: 10.1212/WNL.0b013e3182a4a4af. Epub 2013 Aug 14.

De novo Huntington disease caused by 26-44 CAG repeat expansion on a low-risk haplotype.

Author information

1
From the Center for Medical Genetics and Molecular Medicine (G.H., O.B.), Haukeland University Hospital, Bergen; Section for Medical Genetics (I.B.), Department of Pathology, St. Olavs Hospital, Trondheim, Norway; Centre for Molecular Medicine and Therapeutics (M.R.H., A.S.), Vancouver; and University of British Columbia (M.R.H., A.S.), Vancouver, Canada.
PMID:
23946314
PMCID:
PMC3795589
DOI:
10.1212/WNL.0b013e3182a4a4af
[Indexed for MEDLINE]
Free PMC Article
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