Novel PTCH1 Gene Mutation in a Patient with Gorlin–Goltz Syndrome

Detalles Bibliográficos
Autores principales: Ozlu, Emin, Karadag, Ayse Serap, Akalın, Ibrahim, Yesil, Gozde, Yılmaz, Sarenur, Zindancı, Ilkin, Uzuncakmak, Tugba Kevser, Ozkanlı, Seyma, Akdeniz, Necmettin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Dermatological Association; The Korean Society for Investigative Dermatology 2019
Materias:
Brief Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7997056/
https://www.ncbi.nlm.nih.gov/pubmed/33911679
http://dx.doi.org/10.5021/ad.2019.31.S.S10

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7997056/
https://www.ncbi.nlm.nih.gov/pubmed/33911679
http://dx.doi.org/10.5021/ad.2019.31.S.S10

Ejemplares similares