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)

First Author: Lewis MA
Attributed to:  Sphingosine-1-phosphate signalling in hearing loss funded by MRC

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