Therapeutic approaches to Huntington disease: from the bench to the clinic
Author:
Publisher
Springer Science and Business Media LLC
Subject
Drug Discovery,Pharmacology,General Medicine
Link
http://www.nature.com/articles/nrd.2018.133.pdf
Reference299 articles.
1. Fisher, E. R. & Hayden, M. R. Multisource ascertainment of Huntington disease in Canada: prevalence and population at risk. Mov. Disord. 29, 105–114 (2014). This article describes prevalence estimates for HD in the general population as well as for at-risk individuals and highlights that prevalence was previously underestimated.
2. Evans, S. J. et al. Prevalence of adult Huntington's disease in the UK based on diagnoses recorded in general practice records. J. Neurol. Neurosurg. Psychiatry 84, 1156–1160 (2013).
3. Andrew, S. E. et al. The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease. Nat. Genet. 4, 398–403 (1993).
4. Snell, R. G. et al. Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease. Nat. Genet. 4, 393–397 (1993).
5. Duyao, M. et al. Trinucleotide repeat length instability and age of onset in Huntington's disease. Nat. Genet. 4, 387–392 (1993).
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