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High-throughput sequencing to decipher the genetic heterogeneity of deafness
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.
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| Hoofdauteurs: | , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
BioMed Central
2012
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3446284/ https://ncbi.nlm.nih.gov/pubmed/22647651 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/gb-2012-13-5-245 |
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