• MLYCD Gene Mutation Analysis, Tissue
  • Cholesterol, Body Fluid
  • Human T-Cell Lymphotropic Virus (HTLV) I/II Antibody Screen
  • Hirschsprung Disease
  • Iron deficiency anemia
  • Rhesus D (Rh D), Typing
  • Chronic liver disease
  • Clonazepam, Urine
  • Serotonin Transporter (SLC6A4) Genotyping
  • Inflammatory bowel disease
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /Spinocerebellar Ataxia Type 7 (SCA7) 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 7 (SCA7) Gene Mutation Analysis
Medical Test

Methodology
Access to Spinocerebellar Ataxia Type 7 (SCA7) Gene Mutation Analysis is restricted.
Loading...