Appel à projets Lama2France - « Merosin-deficient Congenital muscular dystrophy»
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Due to the specificities of the field of rare diseases, the LAMA2 France Association and the Fondation Maladies Rares (Foundation For Rare Diseases - FFRD) have agreed on a partnership to support and stimulate research on laminin-alpha2-deficient congenital muscular dystrophy.
The aim of this call is to support any innovative research (basic or translational) aimed at the development of therapeutic strategies. All biomedical disciplines are eligible.
Max budget: 25 000 €
Max duration: 24 months
Deadline: 13/05/2025, 5pm (Paris time).
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Océans - Mondes sociaux, mondes vivants
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(in 63 days)
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