Carbohydrate Deficient Transferrin for Congenital Disorders of Glycosylation, Serum
Paroxetine, Serum
Fatty Acids, Free
NOP10 Gene Mutation Analysis
Rapid Plasma Reagin (RPR), CSF
MLYCD Gene Mutation Analysis, Blood
Lead, Blood
B-Cell Lymphoma, FISH, Bone Marrow
Age Related Macular Degeneration Gene Mutation Analysis
Microsomal epoxide hydrolase 1 (EPHX1) Gene Variation
LDS
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Pompe Disease (GAA) Gene Mutation Analysis
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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
Pompe Disease (GAA) Gene Mutation Analysis
Medical Test
Diseases (1)
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