Myotonic Dystrophy Type 1 19q 13.3
This genetic test detects CTG trinucleotide repeat expansion in the DMPK gene associated with Myotonic Dystrophy Type 1. It confirms diagnosis, predicts disease severity, and assists in family screening and genetic counseling for this progressive neuromuscular disorder.
Myotonic Dystrophy Type 1 19q 13.3
Myotonic Dystrophy Type 1 19q 13.3
