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Volumn 7, Issue 5, 2001, Pages 1149-1153
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Lethal outcome of a patient with a complete dihydropyrimidine dehydrogenase (DPD) deficiency after administration of 5-fluorouracil: Frequency of the common IVS14+1G>A mutation causing DPD deficiency
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Author keywords
[No Author keywords available]
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Indexed keywords
DIHYDROPYRIMIDINE DEHYDROGENASE;
FLUOROURACIL;
ARTICLE;
CANCER PATIENT;
CAUCASIAN;
CONTROLLED STUDY;
DIHYDROPYRIMIDINE DEHYDROGENASE DEFICIENCY;
DRUG METABOLISM;
ENZYME ACTIVITY;
ENZYME DEFICIENCY;
EXON;
GENE FREQUENCY;
GENE MUTATION;
GENETIC ANALYSIS;
GENETIC SCREENING;
HOMOZYGOSITY;
HUMAN;
HUMAN CELL;
LETHALITY;
LEUKOPENIA;
MONONUCLEAR CELL;
POLYMERASE CHAIN REACTION;
PRIORITY JOURNAL;
RESTRICTION FRAGMENT LENGTH POLYMORPHISM;
STOMATITIS;
THROMBOCYTOPENIA;
ADULT;
ANTIMETABOLITES, ANTINEOPLASTIC;
DIHYDROURACIL DEHYDROGENASE (NADP);
EXONS;
FATAL OUTCOME;
FEMALE;
FIBROBLASTS;
FLUOROURACIL;
GENE FREQUENCY;
HUMANS;
LEUKOCYTES, MONONUCLEAR;
MUTATION;
OXIDOREDUCTASES;
POLYMORPHISM, RESTRICTION FRAGMENT LENGTH;
THYMINE;
URACIL;
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EID: 0034901306
PISSN: 10780432
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (264)
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References (25)
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