Study the Role of SHMT1 Polymorphism in Parkinson Disease Clinical Trial
Official title:
Genetic Polymorphisms of Serine Hydroxylmethyl Transferase 1 (SHMT1) in Patients With Parkinson's Disease
Parkinson Disease (PD) is the most common movement disorder and represents the second most common degenerative disease of the central nervous system . SHMT has been shown to be associated with various diseases.
This case -control observational prospective study will conducted on 40 patients with PD. ;