Scientists Detect Probable Genetic Cause of Some Parkinson’s Disease Cases
Two new studies strongly suggest that a mutation in a recently discovered gene is the most common genetic cause of Parkinson’s disease identified to date. The discovery by an international research team provides fresh evidence that genetics may contribute to the development of some cases of Parkinson’s disease. The findings could lead to the development of a genetic test to detect the mutation in individuals at risk. The research team includes investigators at the National Institute on Aging (NIA) and scientists supported by the National Institute of Neurological Disorders and Stroke (NINDS).