Adenovirus Antigen Detection
Hereditary Dilated Cardiomyopathy Gene Mutation Panel, NGS
Desipramine, Serum
Carnitine Palmitoyltransferase II Deficiency, Gene Mutation Analysis
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
LDS
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Solute carrier family 6 member 2 (SLC6A2)
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
Solute carrier family 6 member 2 (SLC6A2)
Medical Test
Overview
Access to
Solute carrier family 6 member 2 (SLC6A2)
is restricted.
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