When access is an issue: exploring barriers to predictive testing for Huntington disease in British Columbia, Canada
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://www.nature.com/articles/ejhg2012147.pdf
Reference36 articles.
1. Walker FO : Huntington’s disease. Lancet 2007; 369: 218–228.
2. MacDonald ME, Ambrose CM, Duyao MP et al. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington’s disease chromosomes. Cell 1993; 72: 971–983.
3. Hayden M : Huntington’s Chorea. New York, NY, USA: Springer-Verlag, 1981.
4. Rae D, Simpson SA : A standard of care for Huntington’s disease: who, what and why. Neurodegen Dis Manage 2012; 2: 1–5.
5. Brandt J, Quaid KA, Folstein SE et al. Presymptomatic diagnosis of delayed-onset disease with linked DNA markers. The experience in Huntington’s disease. JAMA 1989; 261: 3108.
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