Mohamed. S. Khalil

Genetic Analysis of Leucin-Rich Repeat Kinase 2 (LRRK2) G2019S Mutation in a Sample of Egyptian Patients with Parkinson's Disease, a Pilot Study

Ehab. S. El Desoky, Eman. M. Khedr, Mohamed. S. Khalil & Thomas Gasser · Journal of Advances in Medicine and Medical Research · 2014

Aim: Many causative genes and susceptibility loci have been identified to be associated with Parkinson's disease (PD) in different ethnic populations. One of these genes is the Leucin-rich repeat kinase 2 (LRRK2) gene. The G2019S substitution in that gene is the most common mutat...