About

News and press releases about the Joshua Frase Foundation and its efforts behind CNM/MTM

Tue, May 07, 2019

How this promising gene therapy for a rare neuromuscular disease was fueled by passionate parents and a dog


Many treatments for rare diseases begin with families who work tirelessly, sometimes for decades, to fund the initial studies leading to the clinic. For X-linked myotubular myopathy (MTM), an amazing couple and their brave and brilliant son; a team of geneticists, physicians, and veterinarians; and some incredible dogs lie behind the encouraging interim findings presented at the recent American Society of Gene and Cell Therapy annual meeting in Washington, DC.