Movement Disorder Genomic Study (MDGS)

Brief description of study

The purpose of this study is to advance our understanding of the genetic causes of brain disorders, such as movement disorders. Currently, treatment strategies to address movement disorders are largely aimed at symptoms, but not the underlying cause of the disease. Our goal is to increase our knowledge by identifying the genetic causes of these diseases and use this information to help find ways to improve diagnosis and treatment of these diseases.

Clinical Study Identifier: s21-00207

If you are registered as a volunteer, please log in to contact the study team/express interest in this study.