Cytochrome P450 3A7 (CYP3A7) Genotyping
The Enhanced Liver Fibrosis (ELF)
Gonadotropin Releasing Hormone (Gn-RH)
Tropheryma whipplei, Molecular
Legius Syndrome (SPRED1) Sequencing
C3D Circulating Immune Complex Assay
Thiothixene (Navane), Urine
Hepatitis A Virus (HAV) Antibody, IgM
Calcium/Creatinine, 24 Hour, Urine
Troponin-I/T, Cardiac

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/Spinocerebellar Ataxia Type 1 (ATXN1) 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

Spinocerebellar Ataxia Type 1 (ATXN1) Gene Mutation Analysis
Medical Test

Reference Ranges

Access to Spinocerebellar Ataxia Type 1 (ATXN1) Gene Mutation Analysis is restricted.