Hereditary urea cycle abnormalityornithine transcarbamylase deficiency (OTC); citrullinemia; arginase deficiency; argininosuccinic aciduria; carbamyl phosphate
synthetase (CPS) deficiency
... HealthCentral Search ResultsNEJM -- Congenital Glutamine Deficiency with Glutamine
Synthetase Mutations -- New England Journal Of Medicine. Congenital Glutamine Deficiency with
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Synthetase Deficiency : Article by Darius J Adams,
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synthetase (GS) deficiency,
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Synthetase Deficiency:: Late-onset form of partial N-acetylglutamate
synthetase deficiency. [Medline] N-Acetylglutamate Synthe
... Management of Hepatitis C: 20022',5'-oligoadenylate
synthetase concentrations in acute and chronic hepatitis C. J Formos Med Assoc. 1997. May;96(5):314-9.
... HealthCentral Search Resultsglycogen-storage disease type 0, GSD-0, glycogen
synthetase deficiency, aglycogenosis, hypoglycemia with deficiency of liver glycogen
synthetase,
...