Prevalence Study of GJB2 Gene Mutations in Iranian Ethnics

• Hoofdauteurs: Kimia Kahrizi (Auteur), Niloufar Bazzaz-Zadegan (Auteur), Marzieh Mohseni (Auteur), Noushin Nik-Zaat (Auteur), Khadijeh Jalalvand (Auteur), Yaser Riaz-el Hosseini (Auteur), Yousef Shafeghati (Auteur), Sanaz Arzhangi (Auteur), Khalil Javan (Auteur), Hosein Najmabadi (Auteur)
• Formaat: Boek
• Gepubliceerd in: University of Social Welfare and Rehabilitation Sciences, 2007-10-01T00:00:00Z.
• Onderwerpen: article
• Online toegang: Connect to this object online.

Objective: Hereditary hearing loss (HHL) is a very common disorder. When inherited in an autosomal recessive manner, it typically presents as an isolated finding. Interestingly and unexpectedly, in spite of extreme heterogeneity, mutations in one gene, GJB2, are the most common cause of congenital s...