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Research on ataxia and paraplegias
Searching for a diagnostic tool
The present Project is relates to a large group of neurodegenerative rare diseases: hereditary ataxias and familial spastic paraplegias. Their diagnosis is really complex due to the overlap among the clinical forms and also, because of the genetic complexity: more than 200 genes are known. The goal of this project is the development of a diagnostic tool that allows the analysis of all the genes involved in these two groups of disorders in order to achieve a definitive and accurate diagnosis. Continue reading
How to make your funding
INDACEA is based on regular fundings with a minimum of 5€/month to the categories you choose. Nonetheless, you may also fund just one project and even preserving your anonymity. Thus:
1. Regular fanding (to be IND)
2. Anonym funding
3. Fund just one project
Funding just one project
INDACEA is based on regular fundings with a minimum of 5€/month to the categories you choose. Nonetheless, you may also fund just one project. That’s why depending on project’s deadline, the minimum to fund may vary. For example, if a project’s deadline is 3 month from when it was first published in our website, minimu will be of 15€ (5€ x 3 months).
The projects we are currently trying to fund
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