Gjb3 Gene Mutations in Non-Syndromic Hearing Loss of Bloch, Kurd, and Turkmen Ethnicities in Iran

BACKGROUND: Hearing loss (HL) is one of the most common heterogeneous congenital disabilities worldwide. Gap junction protein β-3 (GJB3) gene encodes Connexin31 protein (Cx31). The hereditary type of hearing impairment in this gene are known to cause both autosomal recessive and autosomal dominant f...

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Detalles Bibliográficos
Autores principales: ALIAZAMI, Farnoush, FARHUD, Dariush, ZARIF-YEGANEH, Marjan, SALEHI, Siamak, HOSSEINIPOUR, Azam, SASANFAR, Roxana, ESLAMI, Maryam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2020
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7917519/
https://www.ncbi.nlm.nih.gov/pubmed/33708733
http://dx.doi.org/10.18502/ijph.v49i11.4730

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7917519/
https://www.ncbi.nlm.nih.gov/pubmed/33708733
http://dx.doi.org/10.18502/ijph.v49i11.4730

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