Barth Syndrome – When the Lack of Fair, Equitable and Appropriate Regulatory Review Process Jeopardizes Ultra-Rare Drug Development Barth Syndrome Foundation Executive Director Emily Milligan, and Director of Family Services […]
2023 Mito Town Meeting
Getting the Mito Community Research Ready
As more and more clinical trials are taking place for mitochondrial disease, we want to ensure that you are ready to get involved. Listen in to learn about a new […]
