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Thomas, F., Hennebelle, I., Delmas, C., Lochon, I., Dhelens, C., Garnier Tixidre, C., Bonadona, A., Penel, N., Goncalves, A., Delord, J., Toulas, C., & Chatelut, E. (n.d.). genotyping of a family with a novel deleterious DPYD mutation supports the pretherapeutic screening of DPD deficiency with dihydrouracil/uracil ratio. Clinical pharmacology & therapeutics, 99(2), 235–242. http://access.bl.uk/ark:/81055/vdc_100028496734.0x00005a