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Molecular re-investigation of patients with Huntington's disease in Wessex reveals a family with dentatorubral and pallidoluysian atrophy

✍ Scribed by Connarty, M.; Dennis, N.R.; Patch, C.; Macpherson, J.N.; Harvey, J.F.


Book ID
118771714
Publisher
Springer
Year
1996
Tongue
English
Weight
455 KB
Volume
97
Category
Article
ISSN
0340-6717

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