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MSH3 Polymorphisms and Protein Levels Affect CAG Repeat Instability in Huntington's Disease Mice
Expansions of trinucleotide CAG/CTG repeats in somatic tissues are thought to contribute to ongoing disease progression through an affected individual's life with Huntington's disease or myotonic dystrophy. Broad ranges of repeat instability arise between individuals with expanded repeats,...
Autores principales: | Tomé, Stéphanie, Manley, Kevin, Simard, Jodie P., Clark, Greg W., Slean, Meghan M., Swami, Meera, Shelbourne, Peggy F., Tillier, Elisabeth R. M., Monckton, Darren G., Messer, Anne, Pearson, Christopher E. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585117/ https://www.ncbi.nlm.nih.gov/pubmed/23468640 http://dx.doi.org/10.1371/journal.pgen.1003280 |
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