A novel OTOA mutation in an Italian family with hearing loss
Keywords: ترکیب هتروزیگوت; dB; Decibel; Kb; kilobase; SNP; Single Nucleotide Polymorphism; kDa; kiloDalton; TR; Targeted Resequencing; CNV; Copy-number variation; SNV; single-nucleotide polymorphism; OTOA; Otoancorin; Hearing loss; Non-syndromic; Compound heterozygous;