CureNURR1 Foundation

Our sole and solution-oriented mission is to find a treatment or cure for NR4A2-related disorder and the diverse neurological, motor, behavioural and emotional symptoms that are caused by a deficiency of the important NURR1 protein that it encodes.

We seek to actively connect researchers, pharmaceutical companies and clinicians from around the world in order to facilitate research and accelerate access to novel therapeutics, whilst actively consulting with and advocating for patients and their families.