Trichomonas vaginalis, Molecular
Solute Carrier Family 28 Member 3 (SLC28A3) Genotyping
Protriptyline, Urine
Chronic Lymphocytic Leukemia (CLL) Monitoring, MRD Detection, Blood
Hydroxyzine, Urine
Post-transplant Test for Kidney Acute Rejection (VitaGraft™, Tuteva™)
Pneumocystis jirovecii, Molecular
Alpha 1 Microglobulin, Random, Urine
Cortisol Total, Serum
CaM Kinase II (CaMKII, Calcium-dependent Calmodulin Protein Kinase II) Activation
LDS
Sign up
Log in
LDS
/
Medical Tests
/
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 Testing
Access to
Carnitine Palmitoyltransferase II Deficiency, Gene Mutation Analysis
is restricted.
Sign up now