Clinical Trials for Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy With Fatty Liver and Infantile-onset Cataract Caused by TRAPPC11 Mutations)

Congenital Muscle Disease Study of Patient and Family Reported Medical Information

NCT ID: NCT01403402

The Congenital Muscle Disease Study, also known as CMDPROS, is a long-term research project aimed at understanding various types of congenital muscular dystrophy and related conditions. Over the ne...