KCNMA1 Channelopathy Research Program
Thank you for your contribution to the KCNMA1 Channelopathy Research Program at the University of Maryland School of Medicine. Your support is an important foundation for our research efforts to define and treat this debilitating new neurological disorder.
Donations like these make it possible for my lab to partner directly with patients and their physicians to advance our understanding of KCNMA1-Linked Channelopathy. Our goals are to:
- Characterize new patient-associated KCNMA1 gene variants;
- Discover the basis for the neurological and neuromuscular brain dysfunction that produces seizure, movement disorder, and other symptoms experienced by patients;
- Identify new treatment strategies based on understanding KCNMA1 function in the brain and body.
Click here to make your donation. Please be sure to select ‘KCNMA1 Channelopathy Research Program (SOM)‘ on the dropdown menu!
Thank you for your generosity. It is people like you who make the village of caring that KCNMA1 patients need.
Andrea Meredith, Ph.D.