Mouse screen reveals multiple new genes underlying mouse and human hearing loss.
Ontology highlight
ABSTRACT: Adult-onset hearing loss is very common, but we know little about the underlying molecular pathogenesis impeding the development of therapies. We took a genetic approach to identify new molecules involved in hearing loss by screening a large cohort of newly generated mouse mutants using a sensitive electrophysiological test, the auditory brainstem response (ABR). We review here the findings from this screen. Thirty-eight unexpected genes associated with raised thresholds were detected from our unbiased sample of 1,211 genes tested, suggesting extreme genetic heterogeneity. A wide range of auditory pathophysiologies was found, and some mutant lines showed normal development followed by deterioration of responses, revealing new molecular pathways involved in progressive hearing loss. Several
SUBMITTER: Ingham NJ
PROVIDER: S-EPMC6459510 | biostudies-literature | 2019 Apr
REPOSITORIES: biostudies-literature
ACCESS DATA