3-Hydroxy-3-methylglutaryl coenzyme A lyase deficiency: Postnatal management following prenatal diagnosis by analysis of maternal urine
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference9 articles.
1. Patient with defect in leucine metabolism;Faull;N Engl J Med,1976
2. Lethal hypoglycemia in a child with a deficiency of 3-hydroxy-3-methyl glutarylcoenzyme A lyase;Schutgens;J Pediatr,1979
3. 3-hydroxy-3-methylglutaric aciduria, combined with 3-methylglutaconic aciduria;Wysocki;Clin Chim Acta,1976
4. Organic acid excretion in a patient with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency: facts and artefacts;Duran;Clin Chim Acta,1978
5. 3-hydroxy-3-methylglutaric aciduria: 3-hydroxy-3-methylglutaryl-coenzyme A lyase levels in leucocytes;Wysocki;Clin Chim Acta,1976
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