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European Journal of Dermatology

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X-chromosomal insertions at a recurrent site causing ectodermal dysplasia Volume 19, issue 2, March-April 2009

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Authors
Children’s Hospital, University of Erlangen-Nuernberg, Germany, Department of Pediatrics, Medical University of Innsbruck, Innrain 66, 6020 Innsbruck, Austria

Auteur(s) : Holm Schneider1, Christiane Mühle2 1Children’s Hospital, University of Erlangen-Nuernberg, Germany 2Department of Pediatrics, Medical University of Innsbruck, Innrain 66, 6020 Innsbruck, Austria X-linked hypohidrotic ectodermal dysplasia (XLHED; Christ-Siemens-Touraine syndrome; MIM 305100), the most common form of ectodermal dysplasia, is caused by mutations of the gene EDA (previously ED1), encoding ectodysplasin-A. Recently, Tariq et al. [1] reported in this journal [...]