Lack of association between Connexin 31 (GJB3) alterations and sensorineural deafness in Austria
Author:
Publisher
Elsevier BV
Subject
Sensory Systems
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1. A systematic review of the monogenic causes of Non‐Syndromic Hearing Loss (NSHL) and discussion of Current Diagnosis and Treatment options;Clinical Genetics;2022-09-29
2. Connexin Genes Variants Associated with Non-Syndromic Hearing Impairment: A Systematic Review of the Global Burden;Life;2020-10-28
3. Ginsenoside improves papillary thyroid cancer cell malignancies partially through upregulating connexin 31;The Kaohsiung Journal of Medical Sciences;2018-06
4. Genotypes and phenotypes of a family with a deaf child carrying combined heterozygous mutations in SLC26A4 and GJB3 genes;Molecular Medicine Reports;2016-05-13
5. Identification and genotype/phenotype correlation of mutations in a large German cohort with hearing loss;European Archives of Oto-Rhino-Laryngology;2014-09-12
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