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- Next-generation Sequencing Identified a Novel EDA Mutation in a Chinese Pedigree of Hypohidrotic Ectodermal Dysplasia with Hyperplasia of the Sebaceous Glands
- Advances in the genetic understanding of hypohidrotic ectodermal dysplasia
- Current Genetics in Hair Diseases
- Hypohidrotic Ectodermal Dysplasia with c.28delG Mutation in Ectodysplasin A Gene and Severe Atopic Dermatitis Treated Successfully with Tofacitinib
- Identification of Ectodysplasin Target Genes Reveals the Involvement of Chemokines in Hair Development
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Ectodysplasin research—Where to next?
- A new mutation resulting in the truncation of the TRAF6-interacting domain of XEDAR: a possible novel cause of hypohidrotic ectodermal dysplasia: Figure 1
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
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