Abnormal gene product identified in hereditary dentatorubral–pallidoluysian atrophy (DRPLA) brain
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics
Link
http://www.nature.com/articles/ng0595-99.pdf
Reference33 articles.
1. Smith, J.K., Gonda, V.E. & Malamud, N. Unusual form of cerebellar ataxia: combined dentato-rubral and pallido-Luysian degeneration. Neurology 8, 205–209 (1958).
2. Naito, H. & Oyanagi, S. Familial myoclonus epilepsy and choreoathetosis: hereditary dentatorubral-pallidoluysian atrophy. Neurology 32, 798–807 (1982).
3. Takahashi, H. et al. Hereditary dentatorubral-pallidoluysian atrophy: clinical and pathological variants in a family. Neurology 38, 1065–1070 (1988).
4. Sano, A. et al. Anticipation in hereditary dentatorubral-pallidoluysian atrophy. Hum. Genet. 93, 699–702 (1994).
5. Burke, J.R. et al. The Haw River syndrome: dentatorubropallidoluisian atrophy(DRPLA) in an African-American family. Nature Genet. 7, 521–524 (1994).
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