Ascorbic Acid (Vitamin C)
Hematolymphoid Neoplasm Gene Mutation Panel, NGS
Primidone, Urine
Cortisol, Free and Total, Serum
Runt Related Transcription Factor 1 (RUNX1) Gene Mutation Analysis
Cytomegalovirus (CMV) Antibody, IgM
von Willebrand Disease 2N (Subtype Normandy), Genotyping
Valproic Acid, Total, Serum
Hereditary Hemochromatosis (HFE) Mutation Assay
Aminolevulinic Acid, Urine

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/Medical Tests
/Muscular Dystrophies Gene Mutation Panel, NGS

All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
ICD10
Additional ICD10
References

All
Diseases
Overview
Clinical Utility
Interpretation
Reference Ranges
Methodology
Specimen Collection
Additional Testing
Turnaround Time
CPT
ICD10
Additional ICD10
References

Muscular Dystrophies Gene Mutation Panel, NGS
Medical Test

Reference Ranges

Access to Muscular Dystrophies Gene Mutation Panel, NGS is restricted.