DETECTION OF ABNORMAL SULPHUR‐CONTAINING AMINO ACID EXCRETION IN A MASS URINE‐SCREENING PROGRAMME
Author:
Affiliation:
1. Oliver Latham LaboratoryPsychiatric Centre, North RydeSydney
Publisher
AMPCo
Subject
General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.5694/j.1326-5377.1972.tb116567.x
Reference19 articles.
1. PYRIDOXINE THERAPY IN HOMOCYSTINURIA
2. Procedures for Testing Urine Specimens Dried on Filter Paper
3. Homocystinuria: Metabolism of 535 Methionine;Brenton D. P.;Clin. Sci.,1966
4. Results of Mass Screening for Hyperaminoacidemias in the Newborn Infant;Clow C.;Amer. J. Dis. Child.,1969
5. HOMOCYSTINURIA
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1. Chaperone therapy for homocystinuria: the rescue of CBS mutations by heme arginate;Journal of Inherited Metabolic Disease;2014-10-21
2. Homocystinuria;Ergebnisse der Inneren Medizin und Kinderheilkunde / Advances in Internal Medicine and Pediatrics;1982
3. Homocystinuria and Other Methioninemias;Neonatal Screening for Inborn Errors of Metabolism;1980
4. Homocystinuria in New South Wales.;Archives of Disease in Childhood;1978-03-01
5. A screening test for sulphur-containing metabolites in urine using auxotrophic mutants of Escherichia coli K12;Biochemical Medicine;1975-03
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