The Kurt+Peter Foundation funds advanced exon skipping and gene therapy research to develop new treatments for LGMD2C, supporting translational projects at top institutions.
International Research Grants in Congenital Muscular Dystrophy support researchers studying congenital onset laminopathies and dystroglycanopathies to advance treatments, disease understanding, and trial readiness.
Grant Program - Coalition to Cure Calpain 3 supports researchers through calpainopathy research, tool development, and conference travel to advance treatments and clinical trial readiness.
The CDKL5 Pilot Grant Programme from the Loulou Foundation funds innovative research to advance understanding and therapy development for CDKL5 Deficiency Disorder.
General Research Funding - CMT Research Foundation supports researchers and clinicians pursuing translational and discovery research to advance treatments and cures for all types of Charcot-Marie-Tooth disease.
The Jain Foundation funds research projects targeting the mechanisms, diagnosis, and treatment of dysferlinopathies, supporting innovation from basic science to clinical application.