Dmd mdx/Large myd: a new mouse model of neuromuscular diseases useful for studying physiopathological mechanisms and testing therapies

Martins PC, Ayub-Guerrieri D, Martins-Bach AB, et al. Dmdmdx/Largemyd: a new mouse model of neuromuscular diseases useful for studying physiopathological mechanisms and testing therapies. Disease models & mechanisms 2013;6:1167-74   Abstract Although muscular dystrophies are among the most common human genetic disorders, there are few treatment options available. Animal models have become increasingly important for […]