Induced Pluripotent Stem Cell Reprogramming by Integration-Free Sendai Virus Vectors from Peripheral Blood of Patients with Craniometaphyseal Dysplasia

Studies of rare genetic bone disorders are often limited due to unavailability of tissue specimens and the lack of animal models fully replicating phenotypic features. Craniometaphyseal dysplasia (CMD) is a rare monogenic disorder characterized by hyperostosis of craniofacial bones concurrent with a...

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Detalhes bibliográficos
Main Authors: Chen, I-Ping, Fukuda, Keiichi, Fusaki, Noemi, Iida, Akihiro, Hasegawa, Mamoru, Lichtler, Alexander, Reichenberger, Ernst J.
Formato: Artigo
Idioma:Inglês
Publicado em: Mary Ann Liebert, Inc. 2013
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3848480/
https://ncbi.nlm.nih.gov/pubmed/24219578
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/cell.2013.0037
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