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Systematic evaluation of gene variants linked to hearing loss based on allele frequency threshold and filtering allele frequency
As the number of genes identified for linkage to hearing loss has been increasing and more public databases have become available, we aimed to systematically evaluate all variants reported for nonsyndromic hearing loss (NSHL) based on their allele frequencies (AFs) in the general population. Among t...
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| Pubblicato in: | Sci Rep |
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| Autori principali: | , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Nature Publishing Group UK
2019
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6418148/ https://ncbi.nlm.nih.gov/pubmed/30872718 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-019-41068-6 |
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