Functional Characterization of Friedreich Ataxia iPS-Derived Neuronal Progenitors and Their Integration in the Adult Brain

Friedreich ataxia (FRDA) is an autosomal recessive disease characterised by neurodegeneration and cardiomyopathy that is caused by an insufficiency of the mitochondrial protein, frataxin. Our previous studies described the generation of FRDA induced pluripotent stem cell lines (FA3 and FA4 iPS) that...

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Detalles Bibliográficos
Autores principales: Bird, Matthew J., Needham, Karina, Frazier, Ann E., van Rooijen, Jorien, Leung, Jessie, Hough, Shelley, Denham, Mark, Thornton, Matthew E., Parish, Clare L., Nayagam, Bryony A., Pera, Martin, Thorburn, David R., Thompson, Lachlan H., Dottori, Mirella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4084949/
https://www.ncbi.nlm.nih.gov/pubmed/25000412
http://dx.doi.org/10.1371/journal.pone.0101718

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4084949/
https://www.ncbi.nlm.nih.gov/pubmed/25000412
http://dx.doi.org/10.1371/journal.pone.0101718

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