Cargando…
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...
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: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2007
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1896166/ https://www.ncbi.nlm.nih.gov/pubmed/17519034 http://dx.doi.org/10.1186/1471-2164-8-126 |
Ejemplares similares
-
Satellog: A database for the identification and prioritization of satellite repeats in disease association studies
por: Missirlis, Perseus I, et al.
Publicado: (2005) -
Familial frontotemporal dementia with neuronal intranuclear inclusions is not a polyglutamine expansion disease
por: Mackenzie, Ian R, et al.
Publicado: (2006) -
CAG Repeat Not Polyglutamine Length Determines Timing of Huntington’s Disease Onset
Publicado: (2019) -
DNAzyme Cleavage of CAG Repeat RNA in Polyglutamine Diseases
por: Zhang, Nan, et al.
Publicado: (2021) -
Evolution and function of CAG/polyglutamine repeats in protein–protein interaction networks
por: Schaefer, Martin H., et al.
Publicado: (2012)