| Literature DB >> 8858188 |
Abstract
The Huntington's disease mutation and its protein product are widely expressed in the brain, although the link to presumed excitotoxic damage is unknown. The availability of the genetic test increased the study of preclinical changes in the disease and the identification of more rare choreic illnesses. Other types of transient or permanent basal ganglia dysfunction might cause chorea.Entities:
Mesh:
Year: 1996 PMID: 8858188 DOI: 10.1097/00019052-199608000-00010
Source DB: PubMed Journal: Curr Opin Neurol ISSN: 1350-7540 Impact factor: 5.710