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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Detalhes bibliográficos
Main Authors: Papadopoulos, Petros, Viennas, Emmanouil, Gkantouna, Vassiliki, Pavlidis, Cristiana, Bartsakoulia, Marina, Ioannou, Zafeiria-Marina, Ratbi, Ilham, Sefiani, Abdelaziz, Tsaknakis, John, Poulas, Konstantinos, Tzimas, Giannis, Patrinos, George P.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2014
Assuntos:
VI. Genomic variation, diseases and drugs
Acesso em linha: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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