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Solving the Unsolved Rare Diseases

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- Rare Diseases Models & Mechanisms
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WP 2: Novel molecular causes

WP leads:

Alexander Hoischen
Department of Human Genetics, Radboud University Medical Centre, Nijmegen, the Netherlands

Sergi Beltran
Center for Genomic Regulation, Centro Nacional de Análisis Genómico, Barcelona, Spain

Contributing partners:

University of Tübingen (Institute of Medical Genetics and Center of Neurology)
INSERM (Brain & Spine Institute and Institute of Myology)
University College London (Institute of Neurology and Institute of Child Health)
Central Manchester University Hospitals
CHU Dijon
University Hospital Bonn
Instituto de Patologia e Immunologia Molecular da Universidade do Porto (IPATIMUP)
University of Antwerp
University of Newcastle upon Tyne
University of Naples
University of Ferrara
University of Leicester
The Jackson Laboratory

WP2 addresses implementation steps 3-5.

The Project

Welcome
The Project
The Group
Platforms & Tools
- Rare Diseases Models & Mechanisms
Results
Meetings
- Next Meetings
- Past Meetings
News

The Solve-RD project has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement No 779257.

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