Associated Papers
Defective NaCl Reabsorption in Salivary Glands of Eda-Null X-LHED Mice.
Mukaibo T et al.
Journal of Dental Research, 2018
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
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
Hypohidrotic ectodermal dysplasia associated with glucose-6-phosphate dehydrogenase deficiency.
Ermertcan AT et al.
Annals of Dermatology, 2011
[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
Mutation hotspots of SCN9A in primary erythermalgia.
Zhang LL et al.
The British Journal of Dermatology, 2007
X-linked hypohidrotic ectodermal dysplasia mutations in Brazilian families.
Visinoni AF et al.
American Journal of Medical Genetics. Part A, 2003
Mutations in the ED1 gene in Japanese families with X-linked hypohidrotic ectodermal dysplasia.
Hashiguchi T et al.
Experimental Dermatology, 2003
A frameshift mutation of the ED1 gene in sibling cases with X-linked hypohidrotic ectodermal dysplasia.
Nishibu A et al.
Dermatology (basel, Switzerland), 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
X-linked anhidrotic (hypohidrotic) ectodermal dysplasia caused by a novel mutation in EDA1 gene: 406T > G (Leu55Arg)
Martínez F et al.
The Journal of Investigative Dermatology, 1999
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