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

ConclusionThis study confirmsGRXCR2 as a HI ‐associated gene.GRXCR2 should be included to the currently available TGE panels for HI diagnosis.

Source: Molecular Genetics & Genomic Medicine - February 2, 2021 Category: Genetics & Stem Cells Authors: Ambroise Wonkam, Kamogelo Lebeko, Shaheen Mowla, Jean Jacques Noubiap, Mike Chong, Guillaume Pare Tags: ORIGINAL ARTICLE Source Type: research