EVENT DESCRIPTION
Participants to the twelfth MPN&MPNr-EuroNet meeting will have the opportunity to hear from international experts about the newest developments in the molecular diagnosis of MPNs and related congenital/hereditary diseases.
EVENT CONTENT
- to share information on the newest developments in MPNs and related congenital diseases, hereditary erythrocytosis and hereditary thrombocytosis;
- to exchange and diffuse the latest information and recommendations on the molecular assays developed for diagnosis or research in laboratories working on MPNs and related diseases across Europe. NGS will be a special focus of this meeting;
- to provide recommendations for the molecular diagnosis of MPN, hereditary erythrocytosis and hereditary thrombocytosis;
- to discuss and plan for the various tasks and objectives of the three MPN&MPNr-EuroNet working groups (WG);
- to help and mentor young scientists interested in MPNs.