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 journalArticle

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

Van Kuilenburg, A. B. P., Vreken, P., Riva, D., Botteon, G., Abeling, N. G. G. M., Bakker, H. D., & Van Gennip, A. H. (1999). Clinical and biochemical abnormalities in a patient with dihydropyrimidine dehydrogenase deficiency due to homozygosity for the C29R mutation. Journal of Inherited Metabolic Disease, 22(2), 191-192. https://doi.org/10.1023/A:1005470524203

Clinical and biochemical abnormalities in a patient with dihydropyrimidine dehydrogenase deficiency due to homozygosity for the C29R mutation. / Van Kuilenburg, A. B P; Vreken, P.; Riva, D.; Botteon, G.; Abeling, N. G G M; Bakker, H. D.; Van Gennip, A. H.

In: Journal of Inherited Metabolic Disease, Vol. 22, No. 2, 1999, p. 191-192.

Research output: Contribution to journalArticle

Van Kuilenburg, A. B P ; Vreken, P. ; Riva, D. ; Botteon, G. ; Abeling, N. G G M ; Bakker, H. D. ; Van Gennip, A. H. / Clinical and biochemical abnormalities in a patient with dihydropyrimidine dehydrogenase deficiency due to homozygosity for the C29R mutation. In: Journal of Inherited Metabolic Disease. 1999 ; Vol. 22, No. 2. pp. 191-192.
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