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-Reference-Cited by-同舟云学术

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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

Published:2001-10-01 Issue:10 Volume:38 Page:36e-36
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:
Short-container-title:

Author:

Mustapha M.

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Cited by 45 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. Drug-induced hypersensitivity reactions in a Lebanese outpatient population: A decade-long retrospective analysis (2012-2021);Journal of Allergy and Clinical Immunology: Global;2024-02

2. 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

3. Deafness in an auditory specialist, the big brown bat (Eptesicus fuscus);Hearing Research;2021-12

4. GJB2 Mutations Linked to Hearing Loss Exhibit Differential Trafficking and Functional Defects as Revealed in Cochlear-Relevant Cells;Frontiers in Cell and Developmental Biology;2020-04-02

5. Post-lingual non-syndromic hearing loss phenotype: a polygenic case with 2 biallelic mutations in MYO15A and MITF;BMC Medical Genetics;2020-01-02

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