Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases-Reference-Cited by-同舟云学术

Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases

Published:2010-12-09 Issue:1 Volume:32 Page:70-72
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Cluzeau Céline,Hadj-Rabia Smail,Jambou Marguerite,Mansour Sourour,Guigue Philippe,Masmoudi Sahben,Bal Elodie,Chassaing Nicolas,Vincent Marie-Claire,Viot Géraldine,Clauss François,Manière Marie-Cécile,Toupenay Steve,Le Merrer Martine,Lyonnet Stanislas,Cormier-Daire Valérie,Amiel Jeanne,Faivre Laurence,de Prost Yves,Munnich Arnold,Bonnefont Jean-Paul,Bodemer Christine,Smahi Asma

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference29 articles.

1. Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia;Adaimy;Am J Hum Genet,2007

2. Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locus;Bal;Hum Mutat,2007

3. The anhidrotic ectodermal dysplasia gene (EDA) undergoes alternative splicing and encodes ectodysplasin-A with deletion mutations in collagenous repeats;Bayes;Hum Mol Genet,1998

4. WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes;Bohring;Am J Hum Genet,2009

5. Mutations in EDAR account for one-quarter of non-ED1-related hypohidrotic ectodermal dysplasia;Chassaing;Hum Mutat,2006

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