Epigenomics is the study of how genes are switched on and off in our cells. The EpiGenRare node, part of Rare Disease Research UK, will coordinate research in epigenomics of rare diseases, focusing on linking genetic and epigenomic data, understanding common mechanisms and testing therapeutic approaches. The node hopes to address several unmet needs in order to accelerate diagnosis and treatments.

Epigenomics of Rare Disorders (EpiGenRare) Node
Category
- Research programmes and networks
Functions
- Patient and Public Involvement and Engagement (PPIE)
- Research and development





