Dihydropyrimidine dehydrogenase deficiency — A further case
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01811485
Reference4 articles.
1. Bakkeren, J. A. J. M., DeAbreu, R. A., Sengers, R. C. A., Gabreëls, F. J. M., Maas, J. M. and Renier, W. O. Elevated urine, blood and cerebrospinal fluid levels of uracil and thymine in a child with dihydrothymine dehydrogenase deficiency.Clin. Chim. Acta 140 (1984) 247–256
2. Berger, R., Stoker-de Vries, S. A., Wadman, S. K., Duran, M., Beemer, F. A., de Bree, P. K., Weits-Binnerts, J. J., Penders, T. J. and van der Woude, J. K. Dihydropyrimidine dehydrogenase deficiency leading to thymine-uraciluria. An inborn error of pyrimidine metabolism.Clin. Chim. Acta 141 (1984) 227–234
3. Berglund, G., Greter, J., Lindstedt, S., Steen, G., Waldestrom, J. and Weiss, U. Urinary excretion of thymine and uracil in a two year old child with a malignant tumour of the brain.Clin. Chem. 25 (1979) 1325–1328
4. Piper, A. A., Tattersall, M. H. N. and Fox, R. M. The activities of thymidine metabolising enzymes during the cell cycle of a human lymphocyte cell line LAZ-007 synchronised by centrifugal elutriation.Biochim. Biophys. Acta 633 (1980) 400–409
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