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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

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