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High-throughput sequencing to decipher the genetic heterogeneity of deafness
Zippora Brownstein1, Yoni Bhonker, Karen B Avraham
1Department of Human Molecular Genetics and Biochemistry, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv 69978, Israel.
Genome Biology
|June 1, 2012
Abstract:
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.

