| Literature DB >> 6325322 |
Abstract
Huntington disease is a neurological autosomal dominant disease of unknown origin and the search for a suitable diagnostic marker has been extended to the peripheral tissues. It is generally believed that a membrane defect exists in Huntington disease although the evidence is controversial. It is the aim of this review to examine the validity of these claims for each of the peripheral tissues and techniques involved, and it is not intended to include all other aspects of research into Huntington disease.Entities:
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Year: 1984 PMID: 6325322 DOI: 10.1007/bf00286586
Source DB: PubMed Journal: Hum Genet ISSN: 0340-6717 Impact factor: 4.132