GJB4 and GJC3 variants in non-syndromic hearing impairment in Ghana
Author:
Affiliation:
1. West African Centre for Cell Biology of Infectious Pathogens (WACCBIP), University of Ghana, Accra LG 54, Ghana
2. Division of Human Genetics, Faculty of Health Sciences, University of Cape Town, Cape Town 7925, South Africa
Abstract
Funder
Wellcome Trust
National Human Genome Research Institute
Publisher
SAGE Publications
Subject
General Biochemistry, Genetics and Molecular Biology
Link
http://journals.sagepub.com/doi/pdf/10.1177/1535370220931035
Reference73 articles.
1. Differential Diagnosis of Children with Suspected Childhood Apraxia of Speech
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4. Aetiology of childhood hearing loss in Cameroon (sub-Saharan Africa)
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1. Mechanisms of Diseases Associated with Mutation in GJC2/Connexin 47;Biomolecules;2023-04-21
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3. Whole exome sequencing reveals a biallelic frameshift mutation in GRXCR2 in hearing impairment in Cameroon;Molecular Genetics & Genomic Medicine;2021-02-02
4. Connexin Genes Variants Associated with Non-Syndromic Hearing Impairment: A Systematic Review of the Global Burden;Life;2020-10-28
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