Hairless Gene Nonsense Mutations in Alopecia Universalis: A Case Report

• Główni autorzy: Hamed Heidary (Autor), Ali Mardi (Autor), Seyyed Mohammad Mousavi (Autor), Ghasem Khazaie (Autor), Fereshteh Golab (Autor)
• Format: Książka
• Wydane: Tehran University of Medical Sciences, 2021-06-01T00:00:00Z.
• Hasła przedmiotowe: article
• Dostęp online: Connect to this object online.

Alopecia universalis (AU) congenital, known as generalized atrichia, is a severe form of autosomal recessive alopecia that results in complete hair loss of scalp and body. Mutations in the human hairless gene (HR) are associated with the phenotype of the disease. A consanguineous couple who had a ch...