The Mito Foundation is excited to make funds available to exceptional research into mitochondrial disease (mito) as part of its new Medical and Research Funding Strategy. This has been made possible by the fundraising efforts of the Foundation, including The Bloody Long Walk National Series.
Mito Foundation Booster Grants offer an exciting opportunity for those whose research was deemed of a high quality by the National Health and Medical Research Council (NHMRC) but were unsuccessful in securing funding. In addition to awarding up to $75,000 worth, Mito Foundation Booster Grants may assist in securing future NHMRC funding.
Funded Booster Grants
Engineering of molecular tools to correct disease-causing mutations in mitochondrial DNA for Leber’s Hereditary Optic Neuropathy
01/01/2020 → 31/12/2022
Leber’s hereditary optic neuropathy (LHON) is the most common mitochondrial DNA disease, causing optic nerve degeneration and devastating blindness in…
16/04/2018 → 15/04/2019
New genomic technologies are transforming diagnosis of mitochondrial disease (mito) and other inherited diseases but perhaps half of all children…
01/06/2018 → 30/06/2019
The lack of knowledge about mitochondrial disease (mito) means that it is extremely difficult to assess the effectiveness of treatments…
01/02/2019 → 01/02/2021
Dysfunctional mitochondria cause a diverse group of multi-system human pathologies that often result in severe, progressive and lethal diseases for…
Funding Round and Applications
Submit Your Application
Please download the application form below and once completed, please send your application to email@example.com
Please call us on (02) 8033 4113 if you have any queries.