ABOUT THE PROJECT
“Solve-RD – solving the unsolved rare diseases” is a research project funded by the European Commission for five years (2018-2023), aimed to identify the genetic causes of rare diseases for which a molecular cause is not known yet and to improve diagnostics of rare disease patients through contribution to, participation in and implementation of a “genetic knowledge web” which is based on shared knowledge about genes, genomic variants and phenotypes.
Members of the Hereditary Cancer Group Laura Valle and Gabriel Capellá participate in the ERN GENTURIS SOLVE-RD working group.
European Comission - H2020
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