The study aims to identify variation in inherited material (DNA, Genes) that may cause, or increase the risk of movement disorders. This may occur when many people in a family are affected by a similar movement disorder but also sometimes occur when only one person is affected. Trial team will also study blood markers that may help in diagnosis or in monitoring disease progression. This may improve our ability to diagnose these disorders and help in the development of new treatments.
Principal Investigator: Dr Kathryn Peall, Cardiff University, Collaborators at Southmead Hospital: Dr Konrad Szewczyk-Krolikowski
Planned End Date: 31.03.2024
Local Ref (R&D no): R&D 4590