A genotype-phenotype correlation for GJB2 (connexin 26) deafness
Author:
Publisher
BMJ
Subject
Genetics (clinical),Genetics
Cited by 184 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. Spectrum of genetic variants in 306 patients with non-syndromic hearing loss from Croatia;Croatian Medical Journal;2024-06
2. Machine learning-based longitudinal prediction for GJB2-related sensorineural hearing loss;Computers in Biology and Medicine;2024-06
3. GJB2 p.V37I Mutation Associated With Moderate Nonsyndromic Hearing Loss in an Adult Taiwanese Population;Ear & Hearing;2023-06-05
4. The GJB2 (Cx26) Gene Variants in Patients with Hearing Impairment in the Baikal Lake Region (Russia);Genes;2023-04-28
5. 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
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