• Norpropoxyphene, Urine
  • Heinz Body Stain
  • CD4 Lymphocyte Count
  • Hexosaminidase A (MUGS)
  • Cotinine, Urine
  • CYFRA 21-1 (Cytokeratin 19 Fragment), Serum
  • Dexamethasone Suppression Test (Low Dose)
  • Chromosome Analysis, Sister Chromatid Exchange (SCE) for Bloom Syndrome, Blood
  • Solute Carrier Family 22 (SLC22A5) Gene Mutation Analysis
  • IgG Index, Serum
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /Wilson Disease, (ATP7B) Gene Mutation Analysis
  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • ICD10
  • Additional ICD10
  • References
  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • ICD10
  • Additional ICD10
  • References

Wilson Disease, (ATP7B) Gene Mutation Analysis
Medical Test

Turnaround Time
Access to Wilson Disease, (ATP7B) Gene Mutation Analysis is restricted.