Concordance of DMET Plus genotypes with orthogonal genotyping methods

One approach to circumvent barriers to clinical implementation of pharmacogenetics is to employ pre-prescription genotyping that requires interrogation of multiple pharmacogenetic variants using a high-throughput platform. We compared the performance of the DMET Plus array (1,931 variants in 225 gen...

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Xehetasun bibliografikoak
Egile Nagusiak: Fernandez, C.A., Smith, C., Yang, W., Lorier, R., Crews, K.R., Kornegay, N., Hicks, J.K., Stewart, C.F., Kawedia, J.D., Ramsey, L.B., Liu, C., Evans, W.E., Relling, M.V., Broeckel, U.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2012
Gaiak:
Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC3516299/
https://ncbi.nlm.nih.gov/pubmed/22871999
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/clpt.2012.95
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