The Haw River Syndrome: Dentatorubropallidoluysian atrophy (DRPLA) in an African–American family-Reference-Cited by-同舟云学术

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The Haw River Syndrome: Dentatorubropallidoluysian atrophy (DRPLA) in an African–American family

Published:1994-08 Issue:4 Volume:7 Page:521-524
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Burke James R.,Wingfield Martha S.,Lewis Karen E.,Roses Allen D.,Lee James E.,Hulette Christine,Pericak-Vance Margaret A.,Vance Jeffery M.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0894-521.pdf

Reference18 articles.

1. Farmer, T.W. et al. Ataxia, chorea, seizures and dementia. Pathologic features of a newly defined familial disorder. Arch. Neurol. 46, 774–779 (1989).

2. Nagafuchi, S. et al. Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p. Nature Genet. 6, 14–18 (1994).

3. Koide, R. et al. Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA). Nature Genet. 6, 9–13 (1994).

4. Farmer, T.W., Wingfield, M.S., Jacobson, P.L., Katchinoff, B.L., Lynch, S.A. & Curnes, J.T. Neuroimaging of a new familial disorder. J. Neuroimag. 1, 123–128 (1991).

5. Lizuka, R., Hirayama, K. & Maehara, K.A. Dentato-rubro-pallido-luysian atrophy, a clinico-pathological study. J. Neurol. Neurosurg. Psych. 47, 1288–1298 (1984).

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