A Huntington disease-like neurodegenerative disorder maps to chromosome 20p.

Huntington disease (HD) is an autosomal dominant neurodegenerative disorder characterized by motor disturbance, cognitive loss, and psychiatric manifestations. The disease is associated with a CAG trinucleotide-repeat expansion in the Huntington gene (IT15) on chromosome 4p16.3. One family with a hi...

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Detalhes bibliográficos
Main Authors: Xiang, F, Almqvist, E W, Huq, M, Lundin, A, Hayden, M R, Edström, L, Anvret, M, Zhang, Z
Formato: Artigo
Idioma:Inglês
Publicado em: 1998
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377554/
https://ncbi.nlm.nih.gov/pubmed/9792871
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