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  • Factor H Complement Antigen
  • Cytochrome P450 1A2 (CYP1A2) Genotyping
  • Selenium, 24 Hour, Urine
  • Calcium Sensing Receptor (CASR) Gene Mutation Analysis
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  • /Usher Syndrome, Types 1F and 3 (PCDH15 and CLRN1), 2 Variants
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  • 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

Usher Syndrome, Types 1F and 3 (PCDH15 and CLRN1), 2 Variants
Medical Test

Specimen Collection
Access to Usher Syndrome, Types 1F and 3 (PCDH15 and CLRN1), 2 Variants is restricted.
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