Anticipation and Instability of IT-15 (CAG)N Repeats in Parent-Offspring Pairs with Huntington Disease

Huntington disease (HD) is an autosomal dominant degenerative disorder caused by an expanded and unstable trinucleotide repeat (CAG)n in a gene (IT-15) on chromosome 4. HD exhibits genetic anticipation—earlier onset in successive generations within a pedigree. From a population-based clinical sample...

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Detalhes bibliográficos
Main Authors: Ranen, Neal G., Stine, O. Colin, Abbott, Margaret H., Sherr, Meeia, Codori, Ann-Marie, Franz, Mary Louise, Chao, Nientzu I., Chung, Anneke S., Pleasant, Nicole, Callahan, Colleen, Kasch, Laura M., Ghaffari, Manely, Chase, Gary A., Kazazian, Haig H., Brandt, Jason, Folstein, Susan E., Ross, Christopher A.
Formato: Artigo
Idioma:Inglês
Publicado em: 1995
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1801258/
https://ncbi.nlm.nih.gov/pubmed/7668287
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