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A novel mutation in ABCB6 associated with dyschromatosis universalis hereditaria in a Saudi family

Detalles Bibliográficos
Autores principales:	Aldokhayel, Sara, Nouf, Alballa, Khalid, Aleedan, Faisal, Alsaif, Maram, Alotaibi, Ahmed, Alhumidi, Fahad, Alsaif
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Elsevier 2021
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8727889/ https://www.ncbi.nlm.nih.gov/pubmed/35024399 http://dx.doi.org/10.1016/j.jdcr.2021.11.017

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