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Huntington Disease Phenocopy Is a Familial Prion Disease
Huntington disease (HD) is a common autosomal dominant neurodegenerative disease with early adult–onset motor abnormalities and dementia. Many studies of HD show that huntingtin (CAG)n repeat–expansion length is a sensitive and specific marker for HD. However, there are a significant number of examp...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The American Society of Human Genetics
2001
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1235549/ https://ncbi.nlm.nih.gov/pubmed/11593450 |
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