A new mouse model mimicking the liver symptoms of myotonic dystrophy type 1 — the most prevalent form of adult-onset muscular dystrophy — provides insight into why patients develop fatty liver disease and display hypersensitivity to medications, making treatment difficult. The new model opens...

University of Illinois researchers have uncovered a molecular mechanism that influences muscle weakness in a mouse model of Duchenne Muscular Dystrophy, the most common inherited neuromuscular disease and one of the most severe forms of inherited muscular dystrophies. The genetic disorder causes...