Associated Papers
Novel missense mutations in the tumor necrosis factor domain of Ectodysplasin-A cause non-syndromic tooth agenesis in two Chinese families.
Yang C et al.
Archives of Oral Biology, 2026
Genotypic and phenotypic correlations in tooth agenesis: insights from WNT10A and EDA mutations in syndromic and non-syndromic forms.
Wu Y et al.
Human Genetics, 2024
Non-syndromic tooth agenesis associated with a nonsense mutation in ectodysplasin-A (EDA).
Nikopensius T et al.
Journal of Dental Research, 2013
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
Sweating ability and genotype in individuals with X-linked hypohidrotic ectodermal dysplasia.
Schneider H et al.
Journal of Medical Genetics, 2011
Functional analysis of Ectodysplasin-A mutations causing selective tooth agenesis.
Mues G et al.
European Journal of Human Genetics : Ejhg, 2010
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
[Mutations in the ED1 gene in families with X-linked hypohidrotic ectodermal dysplasia].
Fan HL et al.
Zhonghua Kou Qiang Yi Xue Za Zhi = Zhonghua Kouqiang Yixue Zazhi = Chinese Journal of Stomatology, 2007
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