Cargando...
A Deafness Associated Mutant Human Connexin 26 Improves The Epithelial Barrier In Vitro
A large proportion of recessive non-syndromic hearing loss is due to mutations in the GJB2 gene encoding connexin 26 (Cx26), a component of a gap junction. Within different ethnic groups there are specific common recessive mutations each with a relatively high carrier frequency suggesting a possibil...
Guardado en:
| Autores principales: | , , , , , , , , , , , , |
|---|---|
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
2007
|
| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2845879/ https://ncbi.nlm.nih.gov/pubmed/17581693 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00232-007-9025-0 |
| Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|