Genetic Spectrum of Autosomal Recessive Non-Syndromic Hearing Loss in Pakistani Families-Reference-Cited by-同舟云学术

Genetic Spectrum of Autosomal Recessive Non-Syndromic Hearing Loss in Pakistani Families

Published:2014-06-20 Issue:6 Volume:9 Page:e100146
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Shafique Sobia,Siddiqi Saima,Schraders Margit,Oostrik Jaap,Ayub Humaira,Bilal Ammad,Ajmal Muhammad,Seco Celia Zazo,Strom Tim M.,Mansoor Atika,Mazhar Kehkashan,Shah Syed Tahir A.,Hussain Alamdar,Azam Maleeha,Kremer Hannie,Qamar Raheel

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference53 articles.

1. Autosomal recessive non-syndromic hearing loss in the Lebanese population: prevalence of the 30delG mutation and report of two novel mutations in the connexin 26 (GJB2) gene;M Mustapha;J Med Genet,2001

2. Linkage analysis of progressive hearing loss in five extended families maps the DFNA2 gene to a 1.25-Mb region on chromosome 1p;G Van Camp;Genomics,1997

3. Genetic epidemiology of hearing impairment;NE Morton;Ann N Y Acad Sci,1991

4. An overview of hereditary hearing loss;YA Bayazit;ORL J Otorhinolaryngol Relat Spec,2006

5. Paediatric hearing loss in rural Pakistan;MM Elahi;J Otolaryngol,1998

Cited by 50 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 Variant of FDXR as a Molecular Etiology of Postlingual Post-synaptic Auditory Neuropathy Spectrum Disorder via Mitochondrial Dysfunction: Reiteration of the Correlation between Genotype and Cochlear Implantation Outcomes;Clinical and Experimental Otorhinolaryngology;2024-08-31

2. Autosomal recessive non‐syndromic hearing loss genes in Pakistan during the previous three decades;Journal of Cellular and Molecular Medicine;2024-03-27

3. Clinical experience of next generation sequencing based expanded carrier screening in high‐risk couples from a tertiary healthcare center in Pakistan;Prenatal Diagnosis;2024-03-15

4. Expanding Genotype–Phenotype Correlation of CLCNKA and CLCNKB Variants Linked to Hearing Loss;International Journal of Molecular Sciences;2023-12-03

5. A Short Overview on Hearing Loss and Related Auditory Defects;Auditory System - Function and Disorders;2022-09-28