Associated Papers
A novel EDA variant that causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.
Yao L et al.
Bmc Pregnancy and Childbirth, 2025
Structural insights into pathogenic mechanism of hypohidrotic ectodermal dysplasia caused by ectodysplasin A variants.
Yu K et al.
Nature Communications, 2023
36765055 (PubMed )
Supplement: 41467_2023_36367_MOESM1_ESM.pdf
A novel c.916C>A EDA gene pathogenic variant in a boy with X-linked hypohidrotic ectodermal dysplasia.
Mintoff D et al.
Clinical and Experimental Dermatology, 2021
Pathogenic EDA Mutations in Chinese Han Families With Hypohidrotic Ectodermal Dysplasia and Genotype-Phenotype: A Correlation Analysis.
Han Y et al.
Frontiers in Genetics, 2020
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