A de novo missense mutation in the NC1 domain of type VII collagen leads to dystrophic epidermolysis bullosa

Detalles Bibliográficos
Autores principales: Cheng, Ping, Wu, Yingda, Zhang, Wanlu, Zhang, Yuanyuan, Jia, Weixue, Li, Chengrang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2022
Materias:
Letter to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9326925/
https://www.ncbi.nlm.nih.gov/pubmed/35950135
http://dx.doi.org/10.5114/ada.2022.117525

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9326925/
https://www.ncbi.nlm.nih.gov/pubmed/35950135
http://dx.doi.org/10.5114/ada.2022.117525

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