• FBN1 (Fibrillin-1) Genetic Mutation Analysis
  • Solute Carrier Family 22 (SLC22A5) Gene Mutation Analysis
  • Fluoride, Plasma
  • Potassium, Serum
  • Methemoglobin Reductase, Blood
  • Serotonin Receptor HTR2A Genotyping
  • Zinc, 24 Hour, Urine
  • Lysosomal Acid Lipase, Gene Variation
  • NOTCH3 (CADASIL) Gene Mutations Analysis
  • Ehrlichia chaffeensis Antibody, IgG and IgM, IFA
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /Aspartoacylase (ASPA) Gene Mutation Analysis (Canavan Disease)
  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • LOINC
  • ICD10
  • Additional ICD10
  • References
  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • LOINC
  • ICD10
  • Additional ICD10
  • References

Aspartoacylase (ASPA) Gene Mutation Analysis (Canavan Disease)
Medical Test

References
Access to Aspartoacylase (ASPA) Gene Mutation Analysis (Canavan Disease) is restricted.
Loading...