CAG-encoded polyglutamine length polymorphism in the human genome

BACKGROUND: Expansion of polyglutamine-encoding CAG trinucleotide repeats has been identified as the pathogenic mutation in nine different genes associated with neurodegenerative disorders. The majority of individuals clinically diagnosed with spinocerebellar ataxia do not have mutations within know...

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Autores principales: Butland, Stefanie L, Devon, Rebecca S, Huang, Yong, Mead, Carri-Lyn, Meynert, Alison M, Neal, Scott J, Lee, Soo Sen, Wilkinson, Anna, Yang, George S, Yuen, Macaire MS, Hayden, Michael R, Holt, Robert A, Leavitt, Blair R, Ouellette, BF Francis
Formato: Artigo
Lenguaje:Inglês
Publicado: BioMed Central 2007
Materias:
Research Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC1896166/
https://ncbi.nlm.nih.gov/pubmed/17519034
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-8-126
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