G2019S mutation of the leucine-rich repeat kinase 2 gene in a cohort of Egyptian patients with Parkinson's disease. [electronic resource]
Producer: 20120502Description: 861-6 p. digitalISSN:- 1945-0257
- Aged
- Cohort Studies
- DNA Mutational Analysis
- Egypt -- epidemiology
- Female
- Gene Frequency
- Genetic Predisposition to Disease
- Humans
- Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
- Male
- Middle Aged
- Mutation
- Parkinson Disease -- diagnosis
- Polymerase Chain Reaction -- methods
- Polymorphism, Restriction Fragment Length
- Prevalence
- Protein Serine-Threonine Kinases -- genetics
- Severity of Illness Index
No physical items for this record
Publication Type: Journal Article
There are no comments on this title.
Log in to your account to post a comment.