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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Detalles Bibliográficos
Autores principales: Kuramoto, Takashi, Yokoe, Mayuko, Hashimoto, Ryoko, Hiai, Hiroshi, Serikawa, Tadao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3224228/
https://www.ncbi.nlm.nih.gov/pubmed/22013926
http://dx.doi.org/10.1186/1471-2156-12-91

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3224228/
https://www.ncbi.nlm.nih.gov/pubmed/22013926
http://dx.doi.org/10.1186/1471-2156-12-91

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