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Potential clinical relevance of rare dihydropyrimidine dehydrogenase genetic variants identified using whole-exome NextGen sequencing in cancer patients with severe fluoropyrimidine toxicity

Crossref DOI link: https://doi.org/10.1007/s00280-025-04839-9

Published Online: 2025-12-04

Published Print: 2025-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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