Connexin 26 mutations in autosomal recessive deafness disorders: A review
Author:
Publisher
Informa UK Limited
Subject
Speech and Hearing,Linguistics and Language,Language and Linguistics
Link
http://www.tandfonline.com/doi/pdf/10.1080/14992020600582190
Reference79 articles.
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4. Hearing loss: frequency and functional studies of the most common connexin26 alleles
5. GJB2: The spectrum of deafness-causing allele variants and their phenotype
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1. Divergence between Hemichannel and Gap Junction Permeabilities of Connexin 30 and 26;Life;2023-01-31
2. Connexin26 Modulates the Radiosensitivity of Cutaneous Squamous Cell Carcinoma by Regulating the Activation of the MAPK/NF-κB Signaling Pathway;Frontiers in Cell and Developmental Biology;2021-07-05
3. Novel Mutations in the TMPRSS3 Gene May Contribute to Taiwanese Patients with Nonsyndromic Hearing Loss;International Journal of Molecular Sciences;2020-03-30
4. Concurrent genetic and standard screening test for hearing reduction;Macedonian Pharmaceutical Bulletin;2020
5. Wan Du et al. – Prevalence of GJB2 mutations in the Silk Road region of China and a report of three novel variants. Acta Oto-Laryngol 2014; 134: 373–381;Acta Oto-Laryngologica;2018-03-04
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