Erythrocyte glutathione synthetase in 5-oxoprolinuria: Kinetic studies of the mutant enzyme and detection of heterozygotes
Author:
Publisher
Elsevier BV
Subject
Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine
Reference5 articles.
1. Pyroglutamic Aciduria — a New Inborn Error of Metabolism
2. PYROGLUTAMIC ACIDURIA Studies in an Infant with Chronic Metabolic Acidosis
3. Pyroglutamic Aciduria (5-Oxoprolinuria), an Inborn Error in Glutathione Metabolism
4. On the mechanism of 5-oxoproline overproduction in 5-oxoprolinuria
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1. 5-Oxoproline concentrations in acute acetaminophen overdose;Clinical Toxicology;2019-05-03
2. Acute metabolic crisis with extreme deficiency of glutathione in combination with decreased CSF levels of leukotriene C4 in a patient with glutathione synthetase deficiency;Journal of Inherited Metabolic Disease;2004-03
3. Transient 5-oxoprolinuria (pyroglutamic aciduria) with systemic acidosis in an adult receiving antibiotic therapy;Clinical Chemistry;1998-02-01
4. Prenatal diagnosis of glutathione synthase deficiency;Prenatal Diagnosis;1994-06
5. Glutathione Synthetase Deficiency: A Family Report;Journal of the Royal Society of Medicine;1994-03
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