Associated Papers
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
[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
Mutations in the ED1 gene in Japanese families with X-linked hypohidrotic ectodermal dysplasia.
Hashiguchi T et al.
Experimental Dermatology, 2003
Mutations leading to X-linked hypohidrotic ectodermal dysplasia affect three major functional domains in the tumor necrosis factor family member ectodysplasin-A.
Schneider P et al.
The Journal of Biological Chemistry, 2001
Mutational spectrum of the ED1 gene in X-linked hypohidrotic ectodermal dysplasia.
Vincent MC et al.
European Journal of Human Genetics : Ejhg, 2001
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