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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Bibliografski detalji
Glavni autori: 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
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2007
Teme:
Research Article
Online pristup: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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