Clinical and biochemical abnormalities in a patient with dihydropyrimidine dehydrogenase deficiency due to homozygosity for the C29R mutation

A. B P Van Kuilenburg, P. Vreken, D. Riva, G. Botteon, N. G G M Abeling, H. D. Bakker, A. H. Van Gennip

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)191-192
Number of pages2
JournalJournal of Inherited Metabolic Disease
Volume22
Issue number2
DOIs
Publication statusPublished - 1999

ASJC Scopus subject areas

  • Endocrinology
  • Genetics
  • Genetics(clinical)

Cite this