Tag Archives: myotonic dystrophy
Methylation profile of DMPK gene in myotonic dystrophy type 1 (DM1)
Myotonic dystrophy type 1 (DM1, Steinert’s disease), is the most common muscular dystrophy in adult life, characterized by myotonia (prolonged muscle contractions), muscle weakness, cataract, cardiac disease, gastrointestinal abnormalities, and central nervous system dysfunction. The clinical spectrum
