Webinar on scientific advances in congenital muscular dystrophy due to merosin deficiency
On Wednesday, November 11th at 6 p.m, there will be a webinar on congenital muscular dystrophy due to merosin deficiency and the main lines of research in Spain.
The webinar will be given by the researchers:
- Laura Coch. PhD in Biomedicine from the University of Barcelona and Bachelor of Biotechnology from the Autonomous University of Barcelona.
- Anna Tuset. Graduated in Pharmacy from the University of Barcelona. Specialized in Clinical Research with special interest in observational studies.
Join it to learn in depth about the disease and the evolution of the medical research projects that are underway.
Free access with previous registration.
Currently, the association has accompanied two research projects, thanks to the guidance of the Scientific Committee of the ImpulsaT association and the support of companies, institutions and private donations.
- Development of a new pre-clinical gene therapy strategy for the treatment of congenital muscular dystrophy 1a.
- Uni-large: development of a new gene therapy technology to treat congenital muscular dystrophy type 1a.