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...

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Detaylı Bibliyografya
Asıl Yazarlar: Man, Y.K. Stella, Trolove, Caroline, Tattersall, Daniel, Thomas, Anna C., Papakonstantinopoulou, Annie, Patel, Drashnika, Scott, Claire, Chong, Jiehan, Jagger, Daniel J., O’Toole, Edel A., Navsaria, Harshad, Curtis, Michael A., Kelsell, David P.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2007
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Article
Online Erişim: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
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