• Asymmetric Dimethylarginine, Plasma
  • Phospholamban (PLN) Gene Mutation Analysis
  • Lipoprotein Associated Phospholipase A2 (PLAC)
  • Galactose-1-phosphate Uridyltransferase (GALT) Gene Mutation Analysis
  • Solute carrier family 6 member 2 (SLC6A2)
  • Coagulation Factor VIII Inhibitor Screen, Plasma
  • Myocardial Antibody, IgG
  • Mucolipidosis Type IV (MCOLN1) Mutation Analysis
  • Catechol-O-methyltransferase Genotyping (COMT)
  • Short-Chain Acyl-CoA Dehydrogenase (SCAD) Deficiency, Genetic Mutation Analysis
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  • /Ammonia, Serum
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  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • LOINC
  • ICD10
  • Additional ICD10
  • References

Ammonia, Serum
Medical Test

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