CRISPR/Cas9-mediated correction of MITF homozygous point mutation in a Waardenburg syndrome 2A pig model

Gene therapy for curing congenital human diseases is promising, but the feasibility and safety need to be further evaluated. In this study, based on a pig model that carries the c.740T>C (L247S) mutation in MITF with an inheritance pattern and clinical pathology that mimics Waardenburg syndrome 2...

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Detalles Bibliográficos
Autores principales: Yao, Jing, Wang, Yu, Cao, Chunwei, Song, Ruigao, Bi, Dengfeng, Zhang, Hongyong, Li, Yongshun, Qin, Guosong, Hou, Naipeng, Zhang, Nan, Zhang, Jin, Guo, Weiwei, Yang, Shiming, Wang, Yanfang, Zhao, Jianguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8141604/
https://www.ncbi.nlm.nih.gov/pubmed/34094716
http://dx.doi.org/10.1016/j.omtn.2021.04.009

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8141604/
https://www.ncbi.nlm.nih.gov/pubmed/34094716
http://dx.doi.org/10.1016/j.omtn.2021.04.009

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