High-throughput sequencing to decipher the genetic heterogeneity of deafness
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Genome Biology 2012, 13:245 doi:10.1186/gb-2012-13-5-245Published: 29 May 2012
Identifying genes causing non-syndromic hearing loss has been challenging using traditional approaches. We describe the impact that high-throughput sequencing approaches are having in discovery of genes related to hearing loss and the implications for clinical diagnosis.