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The aim is to find new candidate genes associated with progressive hearing loss

Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data

Dataset ID Description Technology Samples
EGAD00001000198 Illumina Genome Analyzer II Illumina HiSeq 2000 20
Publications Citations
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