Multiple sclerosis in LRRK2 G2019S Parkinson’s disease and isolated nigral degeneration in a homozygous variant carrier - Wise, Adina; Ortega, Roberto A.; Raymond, Deborah; Cervera, Alessandra; Thorn, Emma; Leaver, Katherine; Russell, David S.; Bressman, Susan B.; Crary, John F.; Saunders-Pullman, Rachel (Frontiers in neurology, 2024)
Keywords: genetic; genetic risk; LRRK2; multiple sclerosis; Neurology; Parkinson’s disease; Parkinson’s genes; autoimmune diseases; genetic; LRRK2; Parkinson’s genes; multiple sclerosis; genetic risk; immunology & inflammation; Parkinson’s disease