@article{fd61577ae54a4571a77752b1bae092fd,
title = "High-throughput sequencing to decipher the genetic heterogeneity of deafness",
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.",
keywords = "Deep sequencing, Exome sequencing, Genomics, Hearing loss, Homozygosity mapping, Massive parallel sequencing, Next-generation sequencing",
author = "Zippora Brownstein and Yoni Bhonker and Avraham, {Karen B.}",
note = "Funding Information: Research in the Avraham laboratory for human genomics research is funded by the National Institutes of Health (NIDCD) R01DC011835, I-CORE Center No. 41/11, and the Hedrich Charitable Trust.",
year = "2012",
month = may,
day = "29",
doi = "10.1186/gb-2012-13-5-245",
language = "אנגלית",
volume = "13",
journal = "Genome Biology",
issn = "1474-7596",
publisher = "BioMed Central Ltd.",
number = "5",
}