This section is dedicated specifically to researchers. You will find here the information about the opportunities of rare diseases research funding at the national level in "National RD funding initiatives" and "Next generation sequencing facilities database" that groups sequencing platforms from Europe and Associated countires.
You are here
Home ›
The foundation
In order to guarantee as much research funding as possible into muscular dystrophy and other genetic diseases, the Telethon team works throughout the year and has adopted a management system for the donated funds that is strict and efficient. For every euro raised by Telethon, about eighty euro cents reach the cutting edge laboratories and excellent research centers.
Scientific area
The selection of the best research projects, the funding of dedicated researchers and the foundation and maintenance of its research institutes make Telethon a point of Italian excellence in the world.
Title of the programme: no title
Type of the programme: thematic call for proposals. The Telethon Foundation funds scientific research on genetic disorders
Recurrence of the programme: yearly
Looking for collaborations | Contact | Interactive FAQ |
For more information ABOUT E-Rare please contact:
E-Rare Coordinator
Daria JULKOWSKA
Tel.: +33(0) 1 78 09 80 78
+33(0) 6 20 14 13 81
daria.julkowska@agencerecherche.fr
Agence Nationale de la Recherche - ANR
Health & Biology Department
50 Avenue Daumesnil
75012 Paris, France