Mutations inEDARADDaccount for a small proportion of hypohidrotic ectodermal dysplasia cases
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2133.2010.09670.x/fullpdf
Reference28 articles.
1. So-called ‘anhidrotic ectodermal dysplasia’;Freire-Maia;Int J Dermatol,1980
2. Towards a new classification of ectodermal dysplasias;Lamartine;Clin Exp Dermatol,2003
3. X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein;Kere;Nat Genet,1996
4. The anhidrotic ectodermal dysplasia gene (EDA) undergoes alternative splicing and encodes ectodysplasin-A with deletion mutations in collagenous repeats;Bayes;Hum Mol Genet,1998
5. Involvement of a novel TNF receptor homologue in hair follicle induction;Headon;Nat Genet,1999
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