A comprehensive study to determine heterogeneity of autosomal recessive nonsyndromic hearing loss in Iran-Reference-Cited by-同舟云学术

A comprehensive study to determine heterogeneity of autosomal recessive nonsyndromic hearing loss in Iran

Published:2012-08-17 Issue:10 Volume:158A Page:2485-2492
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Babanejad Mojgan,Fattahi Zohreh,Bazazzadegan Niloofar,Nishimura Carla,Meyer Nicole,Nikzat Nooshin,Sohrabi Elahe,Najmabadi Amin,Jamali Peyman,Habibi Farkhonde,Smith Richard J.H.,Kahrizi Kimia,Najmabadi Hossein

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference40 articles.

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2. Mutation analysis of familial GJB2-related deafness in Iranian Azeri Turkish patients;Bonyadi;Genet Test Mol Biomarkers,2009

3. Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42;Borck;Am J Hum Genet,2011

4. Mutation of COL11A2 causes autosomal recessive nonsyndromic hearing loss at the DFNB53 locus;Chen;J Med Genet,2005

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