Whole exome sequencing reveals a biallelic frameshift mutation in GRXCR2 in hearing impairment in Cameroon.

Ambroise WonkamKamogelo LebekoShaheen MowlaJean Jacques NoubiapMike ChongGuillaume Pare

Published in: Molecular genetics & genomic medicine (2021)

This study confirms GRXCR2 as a HI-associated gene. GRXCR2 should be included to the currently available TGE panels for HI diagnosis.

Keyphrases