Rare Constitutional and hereditary Diseases, Whole Exome Sequence Analysis, NGS
HLA-B*57:01 Genotype, Abacavir Sensitivity
Transferrin and Transferrin Saturation
COL1A1/COL1A2 Genes Variations Analysis
Hepatitis C Virus (HCV) Genotyping
T-Cell Receptor Gene Rearrangement, Flow Cytometry, Bone Marrow
Beta-2 Adrenergic Receptor (ADRB2) Gene Variation
Idiopathic Pulmonary Fibrosis Diagnostic Test (Envisia™)
Actin (Smooth Muscle) Antibody, IgG
Fluphenazine, Serum
LDS
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Spinocerebellar Ataxia Type 2 (ATXN2) 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
Spinocerebellar Ataxia Type 2 (ATXN2) Gene Mutation Analysis
Medical Test
Diseases (3)
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Spinocerebellar Ataxia Type 2 (ATXN2) Gene Mutation Analysis
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