Dallas scientists granted $420K to test gene therapy for rare neurological disease
Childhood-onset striatonigral degeneration is a rare genetic disorder that robs children of the ability to walk and speak by age...
neurological
University of Sheffield spinout company to pioneer novel therapies for genetic neurological diseases | News
BlackfinBio has raised £2.75 million seed investment to advance revolutionary treatments for Hereditary Spastic Paraplegia (HSP). BlackfinBio has raised £2.75...
