Phenotype in parkinsonian and nonparkinsonian LRRK2 G2019S mutation carriers.
Neurology
; 77(4): 325-33, 2011 Jul 26.
Article
in En
| MEDLINE
| ID: mdl-21753163
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Parkinson Disease
/
Phenotype
/
Protein Serine-Threonine Kinases
/
Genetic Predisposition to Disease
/
Heterozygote
/
Mutation
Type of study:
Prognostic_studies
/
Screening_studies
Limits:
Adult
/
Aged
/
Aged80
/
Female
/
Humans
/
Male
/
Middle aged
Language:
En
Journal:
Neurology
Year:
2011
Document type:
Article