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. (2018)
Attributed to:
The underlying mechanisms of aging in the inner ear
funded by
BBSRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1186/s12920-018-0395-1
PubMed Identifier: 30180840
Publication URI: http://europepmc.org/abstract/MED/30180840
Type: Journal Article/Review
Volume: 11
Parent Publication: BMC medical genomics
Issue: 1
ISSN: 1755-8794