Table of Contents
Originally presented on September 10th, 2021 as a part of the DM1 Track at the 2021 Virtual MDF Annual Conference.
Myotonic dystrophy type 1 (DM1) is a complex disease caused by a rare genetic mutation which can affect many systems of the body, producing symptoms that can vary considerably in type and degree from person to person. Learn about the broad range of basic science, studies, clinical trials and other research approaches that are currently being explored to reduce the burden of DM1 for individuals and families.
Presented by Jeffrey Statland, MD.
