• 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
  • Maprotiline, Urine
  • Cytochrome P450 3A7 (CYP3A7) Genotyping
  • c-KIT Mutation Analysis, Blood, Bone Marrow
  • Oxymorphone, Urine
  • Immunoglobulin G (IgG)
  • LDS
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  • /Solute carrier family 6 member 2 (SLC6A2)
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  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • ICD10
  • Additional ICD10
  • References

Solute carrier family 6 member 2 (SLC6A2)
Medical Test

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