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A rat model of hypohidrotic ectodermal dysplasia carries a missense mutation in the Edaradd gene
BACKGROUND: Hypohidrotic ectodermal dysplasia (HED) is a congenital disorder characterized by sparse hair, oligodontia, and inability to sweat. It is caused by mutations in any of three Eda pathway genes: ectodysplasin (Eda), Eda receptor (Edar), and Edar-associated death domain (Edaradd), which enc...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3224228/ https://ncbi.nlm.nih.gov/pubmed/22013926 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2156-12-91 |
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