Becker muscular dystrophy
Secobarbital, Urine
CD8 Lymphocyte Count
Cryptococcosis
TGFBR2 Gene Mutation Analysis
SARS-CoV-2 (COVID-19) Coronavirus, Genotyping
ATP-binding cassette sub-family B member 1 (ABCB1) Genotyping
MLH1 Hypermethylation (Promoter Methylation) Analysis, Tissue
Protein, Total, 24 Hour, Urine
Periodic Acid-Schiff (PAS), Fungus

LDS
Sign up
Log in

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

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

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

Reference Ranges

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