G. H. V. Lenthe

Dihydropyrimidinase deficiency: Confirmation of the enzyme defect in dihydropyrimidinuria

P. Vreken, A. V. van Kuilenburg, H. van Lenthe, 1997, Journal of Inherited Metabolic Disease.

Heterozygosity for a point mutation in an invariant splice donor site of dihydropyrimidine dehydrogenase and severe 5-fluorouracil related toxicity.

P. Vreken, A. V. van Kuilenburg, H. van Lenthe, 1997, European journal of cancer.