Novel Mutations in the Connexin 26 Gene (GJB2) That Cause Autosomal Recessive (DFNB1) Hearing Loss
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics
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1. Genotypic and Allelic Frequencies of GJB2 Variants and Features of Hearing Phenotypes in the Chinese Population of the Dongfeng-Tongji Cohort;Genes;2023-10-27
2. Functional Consequences of Pathogenic Variants of the GJB2 Gene (Cx26) Localized in Different Cx26 Domains;Biomolecules;2023-10-13
3. Degradation of cochlear Connexin26 accelerate the development of age‐related hearing loss;Aging Cell;2023-09-08
4. A Descriptive Observational Study of GJB2 and GJB6 Mutations in Familial Autosomal Recessive Non-syndromic Hearing Impairment;Indian Journal of Otolaryngology and Head & Neck Surgery;2023-07-07
5. GJB2 p.V37I Mutation Associated With Moderate Nonsyndromic Hearing Loss in an Adult Taiwanese Population;Ear & Hearing;2023-06-05
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