FBN1 (Fibrillin-1) Genetic Mutation Analysis
Solute Carrier Family 22 (SLC22A5) Gene Mutation Analysis
Fluoride, Plasma
Potassium, Serum
Methemoglobin Reductase, Blood
Serotonin Receptor HTR2A Genotyping
Zinc, 24 Hour, Urine
Lysosomal Acid Lipase, Gene Variation
NOTCH3 (CADASIL) Gene Mutations Analysis
Ehrlichia chaffeensis Antibody, IgG and IgM, IFA
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Aspartoacylase (ASPA) Gene Mutation Analysis (Canavan Disease)
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
Aspartoacylase (ASPA) Gene Mutation Analysis (Canavan Disease)
Medical Test
References
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Aspartoacylase (ASPA) Gene Mutation Analysis (Canavan Disease)
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