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Precise Excision of the CAG Tract from the Huntingtin Gene by Cas9 Nickases
Huntington's disease (HD) is a progressive autosomal dominant neurodegenerative disorder caused by the expansion of CAG repeats in the first exon of the huntingtin gene (HTT). The accumulation of polyglutamine-rich huntingtin proteins affects various cellular functions and causes selective dege...
Autores principales: | Dabrowska, Magdalena, Juzwa, Wojciech, Krzyzosiak, Wlodzimierz J., Olejniczak, Marta |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5834764/ https://www.ncbi.nlm.nih.gov/pubmed/29535594 http://dx.doi.org/10.3389/fnins.2018.00075 |
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