Genotype and phenotype in patients with dihydropyrimidine dehydrogenase deficiency
Year: 1999
Type: article
Study design: Observational Study
Source: Human Genetics
DOI: 10.1007/pl00008711
Authors: A. B. P. Van Kuilenburg, P. Vreken, N. G. G. M. Abeling, H. D. Bakker, R. Meinsma, H. Van Lenthe, R. A. De Abreu, J. A. M. Smeitink, H. Kayserili, M. Y. Apak, E. Christensen, I. Holopainen, K. Pulkki, D. Riva, G. Botteon, E. Holme, M. Tulinius, W. J. Kleijer, F. A. Beemer, M. Duran, K. E. Niezen-Koning, G. P. A. Smit, C. Jakobs, L. M. E. Smit, U. Moog, L. J. M. Spaapen, A. H. Van Gennip
Institutions: Amsterdam UMC Location University of Amsterdam, Emma Kinderziekenhuis, University of Amsterdam, Istanbul University, Copenhagen University Hospital, University of Turku, Turku University Hospital, Fondazione IRCCS Istituto Neurologico Carlo Besta, University of Gothenburg, Erasmus University Rotterdam, Wilhelmina Children's Hospital, University of Groningen, Maastricht University
Language: English
Subfield: Clinical Biochemistry
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2115435364