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Whole-exome sequencing and its impact in hereditary hearing loss
Next-generation sequencing (NGS) technologies have played a central role in the genetic revolution. These technologies, especially whole-exome sequencing, have become the primary tool of geneticists to identify the causative DNA variants in Mendelian disorders, including hereditary deafness. Current...
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| Yayımlandı: | Genet Res (Camb) |
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| Asıl Yazarlar: | , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Cambridge University Press
2015
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5503681/ https://ncbi.nlm.nih.gov/pubmed/25825321 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1017/S001667231500004X |
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