High carrier frequency of the GJB2 mutation (35delG) in the north of Iran-Reference-Cited by-同舟云学术

High carrier frequency of the GJB2 mutation (35delG) in the north of Iran

Published:2007-06 Issue:6 Volume:71 Page:863-867
ISSN:0165-5876
Container-title:International Journal of Pediatric Otorhinolaryngology
language:en
Short-container-title:International Journal of Pediatric Otorhinolaryngology

Author:

Chaleshtori Morteza Hashemzadeh,Farrokhi Effat,Shahrani Mehrdad,Kheiri Soleiman,Dolati Masoumeh,Rad Laleh Hoghooghi,Pour-Jafari Hamid,Samani Keihan Ghatreh,Chaleshtori Katayoon Safa,Crosby Andrew H.

Publisher

Elsevier BV

Subject

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

Reference27 articles.

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2. A genetic Approach to understanding auditory function;Steel;Nat. Genet.,2001

3. Connexin 26 mutations associated with the most common form of non syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans;Zelante;Hum. Mol. Genet.,1997

4. A genotype-phenotype correlation for GJB2 (connexion 26) deafness;Cryns;J. Med. Genet.,2004

5. GJB2 mutations and degree of hearing loss: a multicenter study;Snoeckx;Am. J. Hum. Genet.,2005

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3. Research Article Mutation analysis of the GJB2 gene of patients with non-syndromic hearing impairment in the Kurdish population in Sulaimani province, Iraq;Genetics and Molecular Research;2023

4. Rare mutations in Atoh1 lead to hearing loss;Gene Reports;2021-09

5. Genetics of Hearing Loss in North Iran Population: An Update of Spectrum and Frequency of GJB2 Mutations;Journal of Audiology and Otology;2019-10-10