Osmolality, Urine
Transthyretin (TTR) Gene Mutation Analysis
Hemoglobin, Free, Plasma
ATPase Copper Transporting Alpha (ATP7A) Genotyping
Antimicrobial Susceptibility Panel, Fungal (Yeast and Molds)
Vitamin E
Anti Mullerian Hormone (AMH)
Oxcarbazepine, Urine
Hepatitis D Virus (HDV) Antigen
Culture, Body Fluid

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/CNBP Genetic Analysis for Myotonic Dystrophy, Type II (DM2)

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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

CNBP Genetic Analysis for Myotonic Dystrophy, Type II (DM2)
Medical Test

Turnaround Time

Access to CNBP Genetic Analysis for Myotonic Dystrophy, Type II (DM2) is restricted.