Population Data on D7S2425 Marker in Five Ethnic Groups of the Iranian Population: A Highly Informative Marker for Molecular Diagnosis of ARNSHL

Population Data on D7S2425 Marker in Five Ethnic Groups of the Iranian Population: A Highly Informative Marker for Molecular Diagnosis of ARNSHL

Background & Aims: SLC26A4 gene mutations are the second identifiable genetic cause of autosomal recessive nonsyndromic hearing loss (ARNSHL) after GJB2 mutations and are currently investigated in molecular diagnosis.In databases, several potential STR markers related to this region have been in...

Full description

Bibliographic Details
Main Authors: Marjan Mojtabavi Naeini, Sadeq Vallian Boroujeni, Morteza Hashemzadeh Chaleshtori
Format: Article
Language:English
Published: Kerman University of Medical Sciences 2014-01-01
Series:Journal of Kerman University of Medical Sciences
Subjects:
d7s2425 marker
slc26a4
autosomal recessive nonsyndromic hearing loss (arnshl)
iranian population
Online Access:https://jkmu.kmu.ac.ir/article_16146_fa6dea2eff656374c096a8741a0d4318.pdf

Internet

https://jkmu.kmu.ac.ir/article_16146_fa6dea2eff656374c096a8741a0d4318.pdf

Similar Items