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Characterization of forebrain neurons derived from late-onset Huntington's disease human embryonic stem cell lines
Huntington's disease (HD) is an incurable neurodegenerative disorder caused by a CAG repeat expansion in exon 1 of the Huntingtin (HTT) gene. Recently, induced pluripotent stem cell (iPSC) lines carrying atypical and aggressive (CAG60+) HD variants have been generated and exhibit disparate mole...
Autores principales: | Niclis, Jonathan C., Pinar, Anita, Haynes, John M., Alsanie, Walaa, Jenny, Robert, Dottori, Mirella, Cram, David S. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3617399/ https://www.ncbi.nlm.nih.gov/pubmed/23576953 http://dx.doi.org/10.3389/fncel.2013.00037 |
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