Lack of correlation between phenotype and genotype for the polymorphically expressed dihydropyrimidine dehydrogenase in a family of Pakistani origin-Reference-Cited by-同舟云学术

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Lack of correlation between phenotype and genotype for the polymorphically expressed dihydropyrimidine dehydrogenase in a family of Pakistani origin

Published:1997-04 Issue:2 Volume:7 Page:161-163
ISSN:0960-314X
Container-title:Pharmacogenetics
language:en
Short-container-title:Pharmacogenetics

Author:

Fernandez-Salguero Pedro M.,Sapone Andrea,Wei Xiaoxiong,Holt John R.,Jones Steve,Idle Jeffrey R.,Gonzalez Frank J.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Pharmacology, Toxicology and Pharmaceutics,Genetics

Cited by 32 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Review of Neurologic and Developmental Conditions Associated with Pediatric Dihydropyrimidine Dehydrogenase Deficiency;Advances in Molecular Pathology;2024-08

2. Dihydropyrimidine Dehydrogenase Deficiency and Implementation of Upfront DPYD Genotyping;Clinical Pharmacology & Therapeutics;2022-06-12

3. Occurrence of Inborn Errors of Metabolism in Newborns, Diagnosis and Prophylaxis;Endocrine, Metabolic & Immune Disorders - Drug Targets;2021-05-04

4. Purine and Pyrimidine Metabolism;Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics;2021

5. Dihydropyrimidine Dehydrogenase Testing prior to Treatment with 5-Fluorouracil, Capecitabine, and Tegafur: A Consensus Paper;Oncology Research and Treatment;2020

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