Clinical, pathological and genetic characteristics of autosomal dominant inherited dynamin 2 centronuclear myopathy Retraction in /10.3892/mmr.2016.5267
Is it cardiac involvement mimicking acute myocardial infarction in idiopathic inflammatory myopathy?
Muscle MRI findings in a one-year-old girl with merosin-deficient congenital muscular dystrophy type 1A due to LAMA2 mutation: A case report
Myoclonic epilepsy with ragged-red fibers: A case report
The de novo missense mutation N117S in skeletal muscle α‑actin 1 causes a mild form of congenital nemaline myopathy