Exome sequencing in infants with congenital hearing impairment: a population-based cohort study
Abstract
Congenital hearing impairment (HI) is the most common sensory impairment and can be isolated or part of a syndrome. Diagnosis through newborn hearing screening and management through early intervention, hearing aids and cochlear implantation is well established in the Australian setting; however understanding the genetic basis of congenital HI has been missing. This population-derived cohort comprised infants with moderate-profound bilateral HI...
Paper Details
Title
Exome sequencing in infants with congenital hearing impairment: a population-based cohort study
Published Date
Dec 12, 2019
Volume
28
Issue
5
Pages
587 - 596
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