The frequency of the homozygote 35delG mutation in the connexin 26 gene in North African with non-syndromic hearing loss: A meta-analysis study
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics
Reference44 articles.
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2. The anatomy and physiology of the ear and hearing;Alberti,2001
3. Spectrum of GJB2 mutations in a cohort of nonsyndromic hearing loss cases from the Kingdom of Saudi Arabia;Al-qahtani;Genet. Test. Mol. Biomarkers,2010
4. Diversity of the causal genes in hearing impaired algerian individuals identified by whole exome sequencing;Ammar-Khodja;Mol. Genet. Genomic Med.,2015
5. Prevalence of deafness-associated connexin-26 (GJB2) and connexin-30 (GJB6) pathogenic alleles in a large patient cohort from Eastern Sicily;Amorini;Ann. Hum. Genet.,2015
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