Mitochondrial M2 Antibody, IgG
Norovirus, EIA, Stool
ACTH Stimulation Test (Cosyntropin)
Metanephrines, Fractionated, 24 Hour, Urine
PPOX Gene Mutation Analysis, Tissue
Trimipramine, Urine
Anthrax DNA by Molecular Method
Hydroxyzine, Urine
Parathyroid Hormone, Fine-Needle Aspiration Biopsy (FNAB), Needle Wash
5-hydroxytryptamine receptor 1A (HTR1A)
LDS
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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
References
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Carnitine Palmitoyltransferase II Deficiency, Gene Mutation Analysis
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