• Paroxysmal Nocturnal Hemoglobinuria (PNH) (CD55, CD59), Flow, Blood
  • Ascorbic Acid (Vitamin C)
  • Methlyenetetrahydrofolate reductase (MTHFR) Mutation Analysis
  • X and Y Aneuploidy Detection, FISH
  • Culture, Dental (Routine)
  • 1,3-Beta-D-Glucan (Fungitell® ß-D Glucan), Serum
  • Splicing Factor 3b Subunit B1 (SF3B1) Gene Mutation Analysis
  • Eastern Equine Encephalitis Antibody, IgM by IFA, Serum
  • Culture, Feces
  • Actinomyces, Molecular Method
  • LDS
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  • /Hereditary Peripheral Neuropathies Gene Mutation Panel, NGS
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  • Interpretation
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  • CPT
  • ICD10
  • Additional ICD10
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  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • ICD10
  • Additional ICD10
  • References

Hereditary Peripheral Neuropathies Gene Mutation Panel, NGS
Medical Test

Reference Ranges
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