Gene Mutations of the Three Ectodysplasin Pathway Key Players (<i>EDA</i>, <i>EDAR</i>, and <i>EDARADD</i>) Account for More than 60% of Egyptian Ectodermal Dysplasia: A Report of Seven Novel Mutations
Ectodermal dysplasia (ED) is a diverse group of genetic disorders caused by congenital defects of two or more ectodermal-derived body structures, namely, hair, teeth, nails, and some glands, e.g., sweat glands. Molecular pathogenesis of ED involves mutations of genes encoding key proteins of major d...
Main Authors: | , , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
MDPI AG
2021-09-01
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Series: | Genes |
Subjects: | |
Online Access: | https://www.mdpi.com/2073-4425/12/9/1389 |