Spectrum of genetic variants in bilateral sensorineural hearing loss

Conclusion: Understanding the genetic basis of HL provides insight for the clinical diagnosis of hearing impairment cases through the utilization of next-generation sequencing (NGS). Our findings contribute to the knowledge of the heterogeneous genetic profile of HL, especially in a population with a high rate of consanguineous marriage in the Arab population.
Source: Frontiers in Genetics - Category: Genetics & Stem Cells Source Type: research