• Carbohydrate Deficient Transferrin for Congenital Disorders of Glycosylation, Serum
  • Paroxetine, Serum
  • Fatty Acids, Free
  • NOP10 Gene Mutation Analysis
  • Rapid Plasma Reagin (RPR), CSF
  • MLYCD Gene Mutation Analysis, Blood
  • Lead, Blood
  • B-Cell Lymphoma, FISH, Bone Marrow
  • Age Related Macular Degeneration Gene Mutation Analysis
  • Microsomal epoxide hydrolase 1 (EPHX1) Gene Variation
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  • /Pompe Disease (GAA) Gene Mutation Analysis
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  • CPT
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  • Additional ICD10
  • References
  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • LOINC
  • ICD10
  • Additional ICD10
  • References

Pompe Disease (GAA) Gene Mutation Analysis
Medical Test

Diseases (1)
Access to Pompe Disease (GAA) Gene Mutation Analysis is restricted.