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Dihydropyrimidine dehydrogenase deficiency leading to thymine‐uraciluria. An inborn error of pyrimidine metabolism
Author(s) -
Wadman S. K.,
Berger R.,
Duran M.,
Bree P. K.,
Stokerde Vries S. A.,
Beemer F. A.,
WeitsBinnerts J. J.,
Penders T. J.,
der Woude J. K.
Publication year - 1985
Publication title -
journal of inherited metabolic disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.462
H-Index - 102
eISSN - 1573-2665
pISSN - 0141-8955
DOI - 10.1007/bf01811484
Subject(s) - university hospital , chemistry , medicine , pediatrics , family medicine