Dihydropyrimidine Dehydrogenase (DPD) Deficiency: Novel Mutations in the DPD Gene
- 1 January 2002
- book chapter
- other
- Published by Springer Science and Business Media LLC in Advances in experimental medicine and biology
- Vol. 486, 247-250
- https://doi.org/10.1007/0-306-46843-3_48
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Genotype and phenotype in patients with dihydropyrimidine dehydrogenase deficiencyHuman Genetics, 1999
- Characterization of the Human Dihydropyrimidine Dehydrogenase GeneGenomics, 1998
- Recommendations for a nomenclature system for human gene mutationsHuman Mutation, 1998
- Inborn errors of pyrimidine degradation: Clinical, biochemical and molecular aspectsJournal of Inherited Metabolic Disease, 1997