Patient-specific naturally gene-reverted induced pluripotent stem cells in recessive dystrophic epidermolysis bullosa

Spontaneous reversion of disease-causing mutations has been observed in some genetic disorders. In our clinical observations of severe generalized recessive dystrophic epidermolysis bullosa (RDEB), a currently incurable blistering genodermatosis caused by loss-of-function mutations in COL7A1 that re...

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Detalhes bibliográficos
Main Authors: Tolar, Jakub, McGrath, John A., Xia, Lily, Riddle, Megan, Lees, Chris J., Eide, Cindy, Keene, Douglas R., Liu, Lu, Osborn, Mark J., Lund, Troy C., Blazar, Bruce R., Wagner, John E.
Formato: Artigo
Idioma:Inglês
Publicado em: 2013
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3989384/
https://ncbi.nlm.nih.gov/pubmed/24317394
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/jid.2013.523
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