Title : Genotype and phenotype in patients with dihydropyrimidine dehydrogenase deficiency.

Pub. Date : 1999 Jan

PMID : 10071185






1 Functional Relationships(s)
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1 An altered beta-alanine, uracil and thymine homeostasis might underlie the various clinical abnormalities encountered in patients with DPD deficiency. beta-Alanine dihydropyrimidine dehydrogenase Homo sapiens