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EDARADD gene

Known as: EDAR-ASSOCIATED DEATH DOMAIN, EDARADD 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Title A rat model of hypohidrotic ectodermal dysplasia carries amissense mutation in the Edaradd gene
Background: Hypohidrotic ectodermal dysplasia (HED) is a congenital disorder characterized by sparse hair, oligodontia, and… 
2017
2017
University of Groningen Mutations in WNT 10 A are present in more than half of isolated hypodontia cases
Background Dental agenesis is the most common, often heritable, developmental anomaly in humans. Mutations in MSX1, PAX9, AXIN2… 
Review
2010
Review
2010
Isolated oligodontia associated with mutations in AXIN2, MSX1, PAX9, and EDARADD
The general aim of this thesis was to broaden our knowledge of the signs and symptoms, genetics, and outcomes of dental implant… 
2009
2009
Studio clinico e molecolare di famiglie italiane affette da displasia ectodermica: analisi dei geni ED1, EDAR ed EDARADD
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