Associated Papers
Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia.
Kovalskaia VA et al.
Orphanet Journal of Rare Diseases, 2026
41645317 (PubMed )
Supplement: 13023_2026_4211_MOESM1_ESM.xlsx › ____1
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
Prenatal ultrasound findings of ectodermal dysplasia: a case report.
Li L et al.
Bmc Pregnancy and Childbirth, 2022
Currently favored sampling practices for tumor sequencing can produce optimal results in the clinical setting.
Pongor LS et al.
Scientific Reports, 2020
32873813 (PubMed )
Supplement: 41598_2020_71382_MOESM6_ESM.xlsx › HR-deficient__BRCA1_mutant
EDA mutation as a cause of hypohidrotic ectodermal dysplasia: a case report and review of the literature.
Huang SX et al.
Genetics and Molecular Research : Gmr, 2015
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