• Acute hepatic failure
  • Calcium Channel Voltage-dependent L Type alpha 1S Subunit (CACNA1S) Gene Mutation Analysis
  • Complement Component C3, Serum
  • Aminolevulinic Acid, Urine
  • Bone Morphogenetic Protein Receptor Type 1A (BMPR1A) Gene Mutation Analysis
  • Estrone, Serum
  • COL1A1/COL1A2 Genes Variations Analysis
  • HBB (Hemoglobin, Subunit Beta) Gene Mutation Analysis
  • HOXB13 (G84E) Gene Mutation Analysis
  • Antibiotic Resistance, Genotyping
  • LDS
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  • /Duchenne/Becker Muscular Dystrophy (DMD) Gene Mutation Analysis
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  • CPT
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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

Duchenne/Becker Muscular Dystrophy (DMD) Gene Mutation Analysis
Medical Test

Interpretation
Access to Duchenne/Becker Muscular Dystrophy (DMD) Gene Mutation Analysis is restricted.