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Defective NaCl Reabsorption in Salivary Glands of Eda-Null X-LHED Mice
Mutations in the ectodysplasin A gene (EDA) cause X-LHED (X-linked hypohidrotic ectodermal dysplasia), the most common human form of ectodermal dysplasia. Defective EDA signaling is linked to hypoplastic development of epithelial tissues, resulting in hypotrichosis, hypodontia, hypohidrosis, and xer...
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| Publicado no: | J Dent Res |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
SAGE Publications
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6151911/ https://ncbi.nlm.nih.gov/pubmed/29913094 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/0022034518782461 |
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