The aim is to find new candidate genes associated with progressive hearing loss
- Type: Other
- Archiver: EGA European Genome-Phenome Archive
Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data
|EGAD00001000198||Illumina Genome Analyzer II Illumina HiSeq 2000||20|
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.
BMC Med Genomics 11: 2018 77