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Finding New Genes for Non-Syndromic Hearing Loss through an In Silico Prioritization Study
At present, 51 genes are already known to be responsible for Non-Syndromic hereditary Hearing Loss (NSHL), but the knowledge of 121 NSHL-linked chromosomal regions brings to the hypothesis that a number of disease genes have still to be uncovered. To help scientists to find new NSHL genes, we built...
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| Hlavní autoři: | , , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Public Library of Science
2010
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2946934/ https://ncbi.nlm.nih.gov/pubmed/20927407 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0012742 |
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