The p.Gly2019Ser is the commonest pathogenic mutation in the LRRK2 gene among Egyptians with familial and sporadic Parkinson's disease
Preprint in Research Square (July 2024)
The most recent citing publications are shown below. View all 6 publications that cite this research output on Dimensions.
Preprint in Research Square (July 2024)
Preprint in Research Square (May 2024)
Article in Journal of Parkinson's Disease (April 2024)