81187 Cnbp gene detc abnor allele
Pathology & Lab
Also known as: CNBP repeat analysis, Myotonic Dystrophy 2 testing
Molecular analysis of the CNBP gene to detect abnormal CCTG repeat expansions associated with Myotonic Dystrophy type 2.
Clinical Context
Used to diagnose Myotonic Dystrophy type 2 in patients with myotonia, muscle weakness, and family history of similar disease.
RVU Breakdown
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Specialties
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