Population and family studies of dihydropyrimidinuria: Prevalence, inheritance mode, and risk of fluorouracil toxicity
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference9 articles.
1. Dihydropyrimidinuria: a new inborn error of pyrimidine metabolism
2. A novel gene family defined by human dihydropyrimidinase and three related proteins with differential tissue distribution
3. Dihydropyrimidinase deficiency presenting in infancy with severe developmental delay
4. Dihydropyrimidinuria: The First Case in Japan
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