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

Internet

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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