• Lactate, Serum
  • Mercury, 24 Hour, Urine
  • Hereditary Hemorrhagic Telangiectasia, ENG Gene Mutation Analysis
  • Triglycerides, Serum
  • Biopsy, Pericardial
  • Salla Disease Mutation Analysis
  • Spinocerebellar Ataxia Type 3 (SCA3) (Machado-Joseph Disease) Gene Mutation Analysis
  • Triazolam, Urine
  • Minimal Residual Disease (MRD) for Early Detection of Cancer Recurrence (Signatera™, Haystack MRD™)
  • PDGFRB/TEL Translocation (5;12) for Chronic Myelomonocytic Leukemia, FISH, Blood
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  • /Niemann-Pick Disease, Types A and B, Gene Mutation Analysis
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  • Additional ICD10
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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

Niemann-Pick Disease, Types A and B, Gene Mutation Analysis
Medical Test

Methodology
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