Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genes

Open Access UCL Research: Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genes https://t.co/e5rY7CLU2b

Exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variant in hearing loss genes https://t.co/zGTpEEAEjX #bmcmedgenomics

RT @Lisa_S_Nolan27: Recently accepted! Whole sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in…

Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genes. https://t.co/vPgNHUO2PZ