Electrolyte Panel, Serum
ATP-binding cassette transporter A1 (ABCA1) Genotyping
Cri-du-chat Syndrome, 5p15.2 Deletion, FISH
Osteocalcin, Serum
Culture, Yeast
Hydrocodone, Urine
Creatinine with Estimated eGFR, Serum
Immunoperoxidase Stain
PLOD1 Gene Mutation Analysis
X-Linked Adrenoleukodystrophy (ABCD1) Gene Mutation Analysis, Blood
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Carnitine-Acylcarnitine Translocase 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-Acylcarnitine Translocase Deficiency, Gene Mutation Analysis
Medical Test
Reference Ranges
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Carnitine-Acylcarnitine Translocase Deficiency, Gene Mutation Analysis
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