• Solute Carrier Family 22 (SLC22A5) Gene Mutation Analysis
  • Heparin-PF4 Antibody (HIT)
  • Bordetella pertussis and Bordetella parapertussis, Molecular
  • Lead, Random, Urine
  • Steroid Sulfatase Gene, Xp22.3 Deletion, FISH
  • Atypical Pneumonia DNA Panel, Sputum
  • Biopsy, Breast (Core Needle Biopsy/Fine Needle Aspiration)
  • Inhibin B
  • Viral Encephalitis Antibody Panel (CSF)
  • Bacterial Culture Identification Panel by MALDI-TOF Technology
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  • /Amyotrophic Lateral Sclerosis Gene Mutation Panel, NGS
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  • 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

Amyotrophic Lateral Sclerosis Gene Mutation Panel, NGS
Medical Test

Specimen Collection
Access to Amyotrophic Lateral Sclerosis Gene Mutation Panel, NGS is restricted.