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A novel KIT mutation in a family with expanded syndrome of piebaldism

Detalles Bibliográficos
Autores principales:	Hamadah, Issam, Chisti, Muzamil, Haider, Mansoor, Al Dosssari, Haya, Alhumaidan, Rawan, Meyer, Brian F., Wakil, Salma M.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Elsevier 2019
Materias:	Case Series
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6630042/ https://www.ncbi.nlm.nih.gov/pubmed/31341943 http://dx.doi.org/10.1016/j.jdcr.2019.01.021

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