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
Lewis, Morag A., Nolan, Lisa S., Cadge, Barbara A., Matthews, Lois J., Schulte, Bradley A., Dubno, Judy R., Steel, Karen P., Dawson, Sally J.Volume:
11
Language:
english
Journal:
BMC Medical Genomics
DOI:
10.1186/s12920-018-0395-1
Date:
December, 2018
File:
PDF, 1.72 MB
english, 2018