Carnitine Palmitoyltransferase II Deficiency, Gene Mutation Analysis
Adenovirus DNA, Real-time PCR, Qualitative
Iron, Serum
Herpes Simplex Virus (HSV) 1 and 2, Immunoblot
Poly A Binding Protein Nuclear 1Gene (PABPN1) Mutation Analysis
Telomere Defects Gene Mutation Panel, NGS
Paroxysmal nocturnal hemoglobinuria
CaM Kinase II (CaMKII, Calcium-dependent Calmodulin Protein Kinase II) Activation
Topiramate, Urine
Fatty Acid Profile, Peroxisomal
LDS
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Familial Hypercholesterolemia and Related Diseases Multi-Gene 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
Familial Hypercholesterolemia and Related Diseases Multi-Gene Panel, NGS
Medical Test
ICD10
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Familial Hypercholesterolemia and Related Diseases Multi-Gene Panel, NGS
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