Role of GJB2 and GJB6 in Iranian Nonsyndromic Hearing Impairment: From Molecular Analysis to Literature Reviews-Reference-Cited by-同舟云学术

Role of GJB2 and GJB6 in Iranian Nonsyndromic Hearing Impairment: From Molecular Analysis to Literature Reviews

Published:2019-06-19 Issue:1 Volume:39 Page:1-12
ISSN:1551-3815
Container-title:Fetal and Pediatric Pathology
language:en
Short-container-title:Fetal and Pediatric Pathology

Author:

Falah Masoumeh¹,Houshmand Massoud¹²,Balali Maryam¹,Asghari Alimohamad³,Bagher Zohreh¹,Alizadeh Rafieh¹,Farhadi Mohammad¹

Affiliation:

1. ENT and Head & Neck Research Center and Department, The Five Senses Institute, Hazrat Rasool Akram Hospital, Iran University of Medical Sciences, Tehran, Islamic Republic of Iran;

2. Department of Medical Genetics, National Institute for Genetic Engineering and Biotechnology, Tehran, Islamic Republic of Iran;

3. Skull Base Research Center, Iran University of Medical Sciences, Tehran, Islamic Republic of Iran

Funder

ENT

Head & Neck Research Center

Department and Iran University of Medical Sciences

Publisher

Informa UK Limited

Subject

General Medicine,Pathology and Forensic Medicine,Pediatrics, Perinatology, and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/15513815.2019.1627625

Reference59 articles.

1. Newborn Hearing Screening — A Silent Revolution

2. A non–syndromic form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q

3. Phenotype/Genotype Correlations in a DFNB1 Cohort With Ethnical Diversity

4. Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss

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3. Analysis of TMIE gene mutations including the first large deletion of exon 1 with autosomal recessive non-syndromic deafness;BMC Medical Genomics;2022-06-16

4. Causal Variants of the GJB6 Gene are Associated with Hearing Loss and Skin Manifestations: A Case Report from Turkey;International Journal of Dermatology and Venereology;2022-02-14

5. Genetic etiology of hearing loss in Iran;Human Genetics;2022-01-20