Tangier disease (Familial alpha-lipoprotein deficiency)
Cytochrome P450 21A2 (CYP21A2) Genotyping
von Willebrand Disease 2N (Subtype Normandy), Genotyping
Acute bronchitis
Autoinflammatory Syndromes (VEXAS syndrome)
Sperm Antibody, IgA and IgG
Porphobilinogen, Urine
Gardnerella vaginalis
Mitochondrial Fission Factor (MFF) Gene Mutation Analysis
Coccidioides By Molecular Method, Body Fluid
LDS
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Progranulin (GRN) Gene Mutation Analysis
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
Progranulin (GRN) Gene Mutation Analysis
Medical Test
References
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Progranulin (GRN) Gene Mutation Analysis
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