Clinical Aspects of Huntington’s Disease
Author:
Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/7854_2013_238
Reference68 articles.
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2. Andrew SE, Goldberg YP, Kremer B et al (1993) The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington’s disease. Nat Genet 4(4):398–403
3. Aylward EH, Sparks BF, Field KM et al (2004) Onset and rate of striatal atrophy in preclinical Huntington disease. Neurology 63(1):66–72
4. Ballard C, Howard R (2006) Neuroleptic drugs in dementia: benefits and harm. Nat Rev Neurosci 7(6):492–500
5. Barbeau A (1970) Parental ascent in the juvenile form of Huntington’s chorea. Lancet 2(7679):937
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