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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5677914/
https://www.ncbi.nlm.nih.gov/pubmed/29263831
http://dx.doi.org/10.1038/s41525-017-0021-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5677914/
https://www.ncbi.nlm.nih.gov/pubmed/29263831
http://dx.doi.org/10.1038/s41525-017-0021-8

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