Using advances in neuroimaging to detect, understand, and monitor disease progression in Huntington’s disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical)
Link
http://www.springerlink.com/index/pdf/10.1602/neurorx.1.2.263
Reference77 articles.
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3. Goldberg YP, Andrews SE, Theilmann J et al. Familial predisposition to recurrent mutations causing Huntington’s disease: genetic risk to sibs of sporadic cases.J Med Genet 30: 987–990, 1993.
4. Nance M and the American College of Medical Genetics/American Society of Human Genetics Huntington’s Disease Genetic Testing Working Group. Laboratory guidelines for Huntington disease genetic testing.Am J Hum Genet 62: 1243–1247, 1998.
5. The Huntington’ s Disease Collaborative Research Group. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington’s disease chromosomes.Cell 72: 971–983, 1993.
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