State of DM2 Research & Ways to Engage

Originally presented on September 10th, 2021 as a part of the DM2 Track at the 2021 Virtual MDF Annual Conference.

Myotonic dystrophy type 2 (DM2) is a complex disease caused by a rare genetic mutation which can affect many systems of the body, producing symptoms that can vary in type and degree from person to person. Learn about the broad range of basic science, clinical studies, and other research approaches that are currently being explored to reduce the burden of DM2 for individuals and families.

Presented by Laura Ranum, PhD.