Epidemiology, etiology, genetic variants in non- syndromic hearing loss in Iran: A systematic review and meta‐analysis-Reference-Cited by-同舟云学术

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Epidemiology, etiology, genetic variants in non- syndromic hearing loss in Iran: A systematic review and meta‐analysis

Published:2023-05 Issue: Volume:168 Page:111512
ISSN:0165-5876
Container-title:International Journal of Pediatric Otorhinolaryngology
language:en
Short-container-title:International Journal of Pediatric Otorhinolaryngology

Author:

Aliazami Farnoush,Gilani Sapideh,Farhud Dariush,Naraghi Mohsen,Afshari Mahdi,Eslami Maryam

Publisher

Elsevier BV

Subject

Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health

Reference38 articles.

1. Nonsyndromic hearing impairment: unparalleled heterogeneity;Van Camp;Am. J. Hum. Genet.,1997

2. Non-syndromic hearing loss and high-throughput strategies to decipher its genetic heterogeneity;Zhong;J. Otol.,2013

3. Non-syndromic hearing loss: clinical and diagnostic challenges;Vona;Med. Genet.,2020

4. Genetic testing for deafness—GJB2 and SLC26A4 as causes of deafness;Smith;J. Commun. Disord.,2002

5. Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy;Delmaghani;Nat. Genet.,2006

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Novel GJB2 mutation c.188delT compound with c.235delC causing non-syndromic hearing loss in a Chinese family: A case report;Medicine;2024-08-16

2. Genetic landscape of hearing loss in prelingual deaf patients of eastern Iran: Insights from exome sequencing analysis;Clinical Genetics;2024-08-06

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