The prevalence of X-linked hypohidrotic ectodermal dysplasia (XLHED) in Denmark, 1995–2010
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics,General Medicine
Reference32 articles.
1. X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein;Kere;Nat. Genet.,1996
2. X-linked and autosomal recessive hypohidrotic ectodermal dysplasia: genotypic-dental phenotypic findings;Clauss;Clin. Genet.,2010
3. Screening of EDA1 gene in X-linked anhidrotic ectodermal dysplasia using DHPLC: identification of 14 novel mutations in Italian patients;Conte;Genet. Test.,2008
4. Mutation screening of the ectodysplasin-a receptor gene EDAR in hypohidrotic ectodermal dysplasia;van der Hout;Eur. J. Hum. Genet.,2008
5. Mutations in EDAR account for one-quarter of non-ED1-related hypohidrotic ectodermal dysplasia;Chassaing;Hum. Mutat.,2006
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