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65-115 - Molecular analysis in Huntington's disease (HD) for predictive testing and clinical confirmation

โœ Scribed by F. Squitien; L. Di Maio; G. Napolitano; S. Cocozza; G. Campanella


Book ID
118512126
Publisher
Elsevier Science
Year
1997
Tongue
English
Weight
274 KB
Volume
42
Category
Article
ISSN
0006-3223

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Huntington's disease (HD) is an autosomal dominant disease characterized by motor disturbance, cognitive loss and psychiatric manifestations, starting between the fourth and the fifth decade, followed by death within 10-20 years of onset of the disease. The disease-causing mutation is an expansion o