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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
VI. Genomic variation, diseases and drugs
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3964978/
https://www.ncbi.nlm.nih.gov/pubmed/24234438
http://dx.doi.org/10.1093/nar/gkt1125

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