Mutations inEDAR account for one-quarter of non-ED1-related hypohidrotic ectodermal dysplasia
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference17 articles.
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2. Gene defect in ectodermal dysplasia implicates a death domain adapter in development
3. Specific missense mutations in NEMO result in hyper-IgM syndrome with hypohydrotic ectodermal dysplasia
4. The Ectodermal Dysplasia Receptor Activates the Nuclear Factor-κB, JNK, and Cell Death Pathways and Binds to Ectodysplasin A
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