Aortic Dysfunction or Dilation (eg, Marfan syndrome, Loeys Dietz syndrome, Ehler Danlos syndrome type IV, arterial tortuosity syndrome) Gene Mutation Panel, NGS
Procainamide, Urine, or Serum
Wilson Disease, (ATP7B) Gene Mutation Analysis
Amyotrophic Lateral Sclerosis Gene Mutation Panel, NGS
Amobarbital, Urine
Son of Sevenless Homolog 1 (SOS1) Gene Mutation Analysis
Mucopolysaccharidosis VI (ARSB) Gene Mutation Analysis
Interferon gamma (IFN-γ) Production by T- Cells Following Exposure to Various Antigens
Escitalopram, Serum
Nudix Hydrolase 15 (NUDT15) Gene Mutation Analysis
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Carnitine Palmitoyltransferase II Deficiency, Gene Mutation Analysis
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
Carnitine Palmitoyltransferase II Deficiency, Gene Mutation Analysis
Medical Test
Additional ICD10
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Carnitine Palmitoyltransferase II Deficiency, Gene Mutation Analysis
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