Genome sequencing as a platform for pharmacogenetic genotyping: a pediatric cohort study

Whole-genome sequencing and whole-exome sequencing have proven valuable for diagnosing inherited diseases, particularly in children. However, usage of sequencing data as a pharmacogenetic screening tool to ensure medication safety and effectiveness remains to be explored. Sixty-seven variants in 19...

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Detalhes bibliográficos
Publicado no:NPJ Genom Med
Main Authors: Cohn, Iris, Paton, Tara A., Marshall, Christian R., Basran, Raveen, Stavropoulos, Dimitri J., Ray, Peter N., Monfared, Nasim, Hayeems, Robin Z., Meyn, M. Stephen, Bowdin, Sarah, Scherer, Stephen W., Cohn, Ronald D., Ito, Shinya
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2017
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5677914/
https://ncbi.nlm.nih.gov/pubmed/29263831
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41525-017-0021-8
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