Prevalence Study of GJB2 Gene Mutations in Iranian Ethnics

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...

Full description

Saved in:
Bibliographic Details
Main Authors: Kimia Kahrizi (Author), Niloufar Bazzaz-Zadegan (Author), Marzieh Mohseni (Author), Noushin Nik-Zaat (Author), Khadijeh Jalalvand (Author), Yaser Riaz-el Hosseini (Author), Yousef Shafeghati (Author), Sanaz Arzhangi (Author), Khalil Javan (Author), Hosein Najmabadi (Author)
Format: Book
Published: University of Social Welfare and Rehabilitation Sciences, 2007-10-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

Internet

Connect to this object online.

3rd Floor Main Library

Holdings details from 3rd Floor Main Library
Call Number: A1234.567
Copy 1 Available