The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss—A twelve year study-Reference-Cited by-同舟云学术

The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss—A twelve year study

Published:2012-08 Issue:8 Volume:76 Page:1164-1174
ISSN:0165-5876
Container-title:International Journal of Pediatric Otorhinolaryngology
language:en
Short-container-title:International Journal of Pediatric Otorhinolaryngology

Author:

Bazazzadegan Niloofar,Nikzat Nooshin,Fattahi Zohreh,Nishimura Carla,Meyer Nicole,Sahraian Shima,Jamali Payman,Babanejad Mojgan,Kashef Atie,Yazdan Hilda,Sabbagh Kermani Farahnaz,Taghdiri Maryam,Azadeh Batool,Mojahedi Faezeh,Khoshaeen Atefeh,Habibi Haleh,Reyhanifar Farahnaz,Nouri Narges,Smith Richard J.H.,Kahrizi Kimia,Najmabadi Hossein

Publisher

Elsevier BV

Subject

Otorhinolaryngology,General Medicine,Pediatrics, Perinatology, and Child Health

Reference22 articles.

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2. Contribution of connexin-26 (GJB2) mutations and founder effect to nonsyndromic hearing loss in India;Ramshankar;J. Med. Genet.,2003

3. GJB2 and GJB6 mutations;Marlin;Arch. Otolaryngol. Head Neck Surg.,2005

4. G. van Camp, R.J.H. Smith, Hereditary hearing loss homepage. Available from: http://www.uia.ac.be/dnalab/hhh, 2011.

5. A non-syndromic form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q;Guilford;Nat. Genet.,1994

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