Associated Papers
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
Novel EDA p.Ile260Ser mutation linked to non-syndromic hypodontia.
Yang Y et al.
Journal of Dental Research, 2013
23625373 (PubMed )
Supplement: ds_10.1177_0022034513487557.pdf
Methylation state of the EDA gene promoter in Chinese X-linked hypohidrotic ectodermal dysplasia carriers.
Yin W et al.
Plos One, 2013
The second deletion mutation in exon 8 of EDA gene in an XLHED pedigree.
Yin W et al.
Dermatology (basel, Switzerland), 2013
Mutations in the EDA gene are responsible for X-linked hypohidrotic ectodermal dysplasia and hypodontia in Chinese kindreds.
Fan H et al.
European Journal of Oral Sciences, 2008
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