In Vitro Expansion of CAG, CAA, and Mixed CAG/CAA Repeats

Polyglutamine diseases, including Huntington’s disease and a number of spinocerebellar ataxias, are caused by expanded CAG repeats that are located in translated sequences of individual, functionally-unrelated genes. Only mutant proteins containing polyglutamine expansions have long been thought to...

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Detalles Bibliográficos
Autores principales: Figura, Grzegorz, Koscianska, Edyta, Krzyzosiak, Wlodzimierz J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Technical Note
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4581269/
https://www.ncbi.nlm.nih.gov/pubmed/26270660
http://dx.doi.org/10.3390/ijms160818741

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4581269/
https://www.ncbi.nlm.nih.gov/pubmed/26270660
http://dx.doi.org/10.3390/ijms160818741

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