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Genome Biol. 2012 May 29;13(5):245. doi: 10.1186/gb-2012-13-5-245.

High-throughput sequencing to decipher the genetic heterogeneity of deafness.

Author information

1
Department of Human Molecular Genetics and Biochemistry, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv 69978, Israel.

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.

PMID:
22647651
PMCID:
PMC3446284
DOI:
10.1186/gb-2012-13-5-245
[Indexed for MEDLINE]
Free PMC Article

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