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Developments in FINDbase worldwide database for clinically relevant genomic variation allele frequencies
FINDbase (http://www.findbase.org) aims to document frequencies of clinically relevant genomic variations, namely causative mutations and pharmacogenomic markers, worldwide. Each database record includes the population, ethnic group or geographical region, the disorder name and the related gene, acc...
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| 主要な著者: | , , , , , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2014
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3964978/ https://ncbi.nlm.nih.gov/pubmed/24234438 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkt1125 |
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