LRRK2 mutations in a clinic-based cohort of Parkinson's disease

European Journal of Neurology

Volumn 13, Issue 12, 2006, Pages 1298-1301

  Scholz, S ^a   Mandel, R J ^b   Fernandez, H H ^b   Foote, K D ^b   Rodriguez, R L ^b   Barton, E ^b   Munson, S ^b   Singleton, A ^a   Okun, M S ^b  

^a NATIONAL INSTITUTE ON AGING   (United States)

^b UNIVERSITY OF FLORIDA   (United States)

Author keywords

Dardarin; G2019S; LRRK2; Parkinson's disease

Indexed keywords

DARDARIN; LEUCINE RICH REPEAT KINASE 2; PROTEIN; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHILD; FEMALE; GENE LOCUS; GENE MUTATION; GENETIC ANALYSIS; GENETIC SCREENING; HETEROZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; MALE; MUTATIONAL ANALYSIS; PARKINSON DISEASE; PARKINSONISM; PHENOTYPE; PRIORITY JOURNAL; SCREENING TEST;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; AMINO ACID SUBSTITUTION; CHILD; COHORT STUDIES; FEMALE; GENE AMPLIFICATION; GENOTYPE; HUMANS; MALE; MIDDLE AGED; MUTATION; PARKINSON DISEASE; PROTEIN-SERINE-THREONINE KINASES;

EID: 33750941013     PISSN: 13515101     EISSN: 14681331     Source Type: Journal    
DOI: 10.1111/j.1468-1331.2006.01472.x     Document Type: Article

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