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International Journal of Pediatric Otorhinolaryngology, ISSN 0165-5876, 2011, Volume 75, Issue 5, pp. 611 - 617
Abstract Objective The purpose of this study was to determine the prevalence of mutations in the GJB2 gene, the GJB6 -D13S1830 deletion and the four common... 
Otolaryngology | Pediatrics | mtDNA mutations | GJB2 | GJB6-D13S1830 | Molecular diagnosis | Non-syndromic hearing loss | South African population | MtDNA mutations | GAP-JUNCTION | MOLECULAR-GENETICS | SENSORINEURAL DEAFNESS | T7511C MUTATION | A1555G MUTATION | AMINOGLYCOSIDE OTOTOXICITY | OTORHINOLARYNGOLOGY | 12S RIBOSOMAL-RNA | NON-SYNDROMIC DEAFNESS | PEDIATRICS | AUTOSOMAL-RECESSIVE DEAFNESS | CARRIER FREQUENCY | Audiometry | Humans | Child, Preschool | Male | Hearing Loss, Sensorineural - epidemiology | Incidence | Young Adult | DNA, Mitochondrial - genetics | Gene Deletion | Polymerase Chain Reaction | Female | African Continental Ancestry Group - genetics | Genetic Predisposition to Disease - epidemiology | Child | Hearing Tests | Severity of Illness Index | Hearing Loss - physiopathology | Risk Assessment | Hearing Loss - epidemiology | Connexins - genetics | Hearing Loss, Sensorineural - genetics | Mutation - genetics | Connexin 26 | Hearing Loss - genetics | Mass Screening | Polymorphism, Restriction Fragment Length | Adolescent | Africa South of the Sahara - epidemiology | Cohort Studies | Hearing Loss, Sensorineural - physiopathology | Polymerase chain reaction | Deafness | GJB2 protein | Mitochondria | Restriction fragment length polymorphism | Mitochondrial DNA | Gene deletion | Single strand conformation polymorphism | Hearing loss
Journal Article