Homozygous Deletion Mutation of the FERMT1 Gene in a Chinese Patient with Kindler Syndrome

Detalles Bibliográficos
Autores principales: Oh, Seung Joon, Kim, Song-Ee, Lee, Sang Eun, Kim, Soo-Chan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Dermatological Association; The Korean Society for Investigative Dermatology 2016
Materias:
Brief Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4969485/
https://www.ncbi.nlm.nih.gov/pubmed/27489438
http://dx.doi.org/10.5021/ad.2016.28.4.503

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4969485/
https://www.ncbi.nlm.nih.gov/pubmed/27489438
http://dx.doi.org/10.5021/ad.2016.28.4.503

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