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A mild phenotype of dihydropyrimidine dehydrogenase deficiency and developmental retardation associated with a missense mutation affecting cofactor binding

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http://pubman.mpdl.mpg.de/cone/persons/resource/persons78015

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;

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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.


Cite as: http://hdl.handle.net/11858/00-001M-0000-0010-5429-A
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