Detection of the GJB2 Mutation in Iranian Children with Hearing Loss Treated with Cochlear Implantation

The 35delG mutation in the gap junction protein, β2, 26kDa (GJB2) gene is the most common mutation that has been found in children with non syndromic hearing loss. Testing for the GJB2 gene mutation is simple and can directly answer the concerns of the parents about cause of the disorder and prognos...

Descripción completa

Detalles Bibliográficos
Autores principales: Peyvandi, AA, Morovvati, S, Rabiee, HR, Ranjbar, R, Ajalloueyan, M, Hassanalifard, M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Macedonian Science of Sciences and Arts 2011
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3776689/
https://www.ncbi.nlm.nih.gov/pubmed/24052698
http://dx.doi.org/10.2478/v10034-011-0013-4

Ejemplares similares

Ejemplares similares