Characterization of Reference Materials for DPYD
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Publisher
Elsevier BV
Reference42 articles.
1. Human polymorphism in drug metabolism: mutation in the dihydropyrimidine dehydrogenase gene results in exon skipping and thymine uracilurea;Meinsma;DNA Cell Biol,1995
2. Familial deficiency of dihydropyrimidine dehydrogenase. Biochemical basis for familial pyrimidinemia and severe 5-fluorouracil-induced toxicity;Diasio;J Clin Invest,1988
3. Increased risk of grade IV neutropenia after administration of 5-fluorouracil due to a dihydropyrimidine dehydrogenase deficiency: high prevalence of the IVS14+1g>a mutation;Van Kuilenburg;Int J Cancer,2002
4. Dutch Pharmacogenetics Working Group (DPWG) guideline for the gene-drug interaction of DPYD and fluoropyrimidines;Lunenburg;Eur J Hum Genet,2020
5. Capecitabine therapy and DPYD genotype;Dean,2012
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1. DPYD Genotyping Recommendations;The Journal of Molecular Diagnostics;2024-07
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