Two Iranian families with a novel mutation inGJB2causing autosomal dominant nonsyndromic hearing loss-Reference-Cited by-同舟云学术

Two Iranian families with a novel mutation inGJB2causing autosomal dominant nonsyndromic hearing loss

Published:2011-04-11 Issue:5 Volume:155 Page:1202-1211
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Bazazzadegan Niloofar,Sheffield Abraham M.,Sobhani Masoomeh,Kahrizi Kimia,Meyer Nicole C.,Van Camp Guy,Hilgert Nele,Abedini Seyedeh Sedigheh,Habibi Farkhondeh,Daneshi Ahmad,Nishimura Carla,Avenarius Matthew R.,Farhadi Mohammad,Smith Richard J.H.,Najmabadi Hossein

Funder

Iranian National Science Foundation

National Institutes of Health (NIH)-NIDCD

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.33209/fullpdf

Reference51 articles.

1. A novel GJB2 mutation p. Asn54His in a patient with palmoplantar keratoderma, sensorineural hearing loss and knuckle pads;Akiyama;J Invest Dermatol,2007

2. G59S mutation in the GJB2 (connexin 26) gene in a patient with Bart-Pumphrey syndrome;Alexandrino;Am J Med Genet Part A,2005