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...
Saved in:
Main Authors: | , , , , , , , , , |
---|---|
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
Call Number: |
A1234.567 |
---|---|
Copy 1 | Available |