Goettig, P. Fässler, Reinhard / Molecular Medicine, Max Planck Institute of Biochemistry, Max Planck Society; Huber, Robert / Structure Research, Max Planck Institute of Biochemistry, Max Planck Society;
Weidensee, S., Goettig, P., Bertone, M., Haas, D., Magdolen, V., Kiechle, M., et al. (2011). A mild phenotype of dihydropyrimidine dehydrogenase deficiency and developmental retardation associated with a missense mutation affecting cofactor binding. Clinical Biochemistry, 44(8-9), 722-724.
