Determination of the frequency of connexin26 mutations in inherited sensorineural deafness and carrier rates in the Tunisian population using DGGE
Author:
Publisher
BMJ
Subject
Genetics (clinical),Genetics
Cited by 25 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. Etiologic Diagnosis of Genetic Hearing Loss in an Ethnically Diverse Deafness Cohort;Audiology and Neurotology;2024-08-23
2. The frequency of the homozygote 35delG mutation in the connexin 26 gene in North African with non-syndromic hearing loss: A meta-analysis study;Meta Gene;2021-06
3. The Genetic Epidemiology of Orphan Diseases in North Africa;The Genetics of African Populations in Health and Disease;2019-12-19
4. Elucidation of the unique mutation spectrum of severe hearing loss in a Vietnamese pediatric population;Scientific Reports;2019-02-07
5. Genetics and genomic medicine in Tunisia;Molecular Genetics & Genomic Medicine;2018-03
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