Inborn errors of the purine nucleotide cycle: Adenylosuccinase deficiency
Author:
Affiliation:
1. ; Laboratory of Physiological Chemistry; International Institute of Cellular and Molecular Pathology; UCL 7539 Brussels B-1200 Belgium
2. ; Department of Pediatrics; University of Leuven; Leuven B-3000 Belgium
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1005304722259/fullpdf
Reference34 articles.
1. Cloning of a cDNA encoding adenylosuccinate lyase by functional complementation in Escherichia coli;Aimi;J Biol Chem,1990
2. Kinetic studies of mutant human adenylosuccinase;Barshop;Biochim Biophys Acta,1989
3. A new coupling component for sulfanilamide determination;Bratton;J Biol Chem,1939
4. Diagnosis of inherited adenylosuccinase deficiency by thin-layer chromatography of urinary imidazoles and by automated cation exchange column chromatography of purines;De Bree;Clin Chim Acta,1986
5. Regional brain glucose utilization in adenylosuccinase-deficient patients measured by positron emission tomography;De Volder;Pediatr Res,1988
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