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10-05-2023 - Fondation Maladies Rares Partner With Association VMOV for Call for Proposals on Growth Deficiency in Osteogenesis Imperfecta
Fondation Maladies Rares and Association VMOV have made funding available for projects researching growth deficiency caused by osteogenesis imperfecta. The call is open to researchers based in French academic institutions.
The Fondation Maladies Rares (Foundation for Rare Diseases) is a non-profit umbrella organisation created in 2012. Its overall mission is to promote, coordinate and support research on rare diseases to alleviate the social and therapeutic isolation of individuals afflicted with rare diseases and thus improve their daily life.
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