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Deafness (2)
Hearing loss (2)
African populations (1)
Autosomal recessive nonsyndromic hearing loss (1)
Compound heterozygous (1)
DFNB2 (1)
DFNB28 (1)
Gap-junction protein β 2 (GJB2) (1)
Gap-junction protein β 6 (GJB6) (1)
Genetic (1)
Genetics (1)
Homozygous (1)
Indigenous South Africans (1)
MYO7A gene (1)
Next generation sequencing (NGS) (1)
Recessive hearing loss (1)
South African population (1)
Spectrum of DNA (1)
Spectrum of MYO7A mutations (1)
Sub-Saharan Africa (SSA) (1)
TRIOBP R1 and R2 repeat motifs (1)
Usher Type 1B (USH1B) (1)
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