Dihydropyrimidinase deficiency: Confirmation of the enzyme defect in dihydropyrimidinuria
SourceJournal of Inherited Metabolic Disease, 20, (1997), pp. 339-342
Article / Letter to editor
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Journal of Inherited Metabolic Disease
SubjectAsphyxia Neonatorum; Brain; Bronchopulmonary Dysplasia; Central Nervous System Diseases; Hemorrhagic Disease of Newborn; Infant, Newborn, Diseases; Infant, Premature, Diseases; Microcirculation; Netherlands; Neurophysiology; Respiratory Distress Syndrome
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