Familial Hypercholesterolemia and Related Diseases Multi-Gene Panel, NGS
Alpha 1 Microglobulin, Random, Urine
X-Linked Adrenoleukodystrophy (ABCD1) Gene Mutation Analysis, Blood
Adult T-cell leukemia/lymphoma
Dementia With Lewy Bodies
B-Cell Acute Lymphoblastic Leukemia (ALL), FISH, Blood
Autoinflammatory Primary Immunodeficiency (PID) Gene Panel
Telomere Defects Gene Mutation Panel, NGS
Maprotiline, Urine
Oxazepam, Urine

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/Medical Tests
/Carnitine Palmitoyltransferase 1A (CPT1A) 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 1A (CPT1A) Mutation Analysis
Medical Test

Additional Testing

Access to Carnitine Palmitoyltransferase 1A (CPT1A) Mutation Analysis is restricted.