Call for research projects: MTFMT gene and Leigh syndrome

The French Foundation for Rare Diseases (FFRD) in parternship with Association contre les Maladies Mitochondriales (AMMi) are supporting and stimulating biomedical research on MTFMT gene and Leigh syndrome.

In the context of the partnership, a call for research projects to develop research on Leigh syndrome and the MTFMT gene is currently open and will close on August 31st at 17:00 CET. All biomedical disciplines are eligible.

This call for research projects provides for financial support of up to € 10,000 for a maximum
duration of 18 months

More information and application process here: