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- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- Next-generation Sequencing Identified a Novel EDA Mutation in a Chinese Pedigree of Hypohidrotic Ectodermal Dysplasia with Hyperplasia of the Sebaceous Glands
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- A novel EDA variant that causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Myodegeneration in EDA-A2 Transgenic Mice Is Prevented by XEDAR Deficiency
- Edar Signaling in the Control of Hair Follicle Development
- A new mutation resulting in the truncation of the TRAF6-interacting domain of XEDAR: a possible novel cause of hypohidrotic ectodermal dysplasia: Figure 1
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
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