Genetic and clinical identification of Parkinson's disease patients with LRRK2 G2019S mutation [3]

Annals of Neurology

Volumn 57, Issue 6, 2005, Pages 933-934

  Deng, Hao ^a   Le, Weidong ^a   Guo, Yi ^b   Hunter, Christine B ^a   Xie, Wenjie ^a   Jankovic, Joseph ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b CENTRAL SOUTH UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA;

ADULT; AGED; CONTROLLED STUDY; DJ 1 GENE; FEMALE; GENE; GENE FREQUENCY; GENE LOCUS; GENE MUTATION; GENETIC IDENTIFICATION; GENOTYPE PHENOTYPE CORRELATION; HUMAN; LETTER; LRRK2 GENE; MAJOR CLINICAL STUDY; MALE; PARKIN GENE; PARKINSON DISEASE; PATHOGENESIS; PINK1 GENE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SCNA GENE;

AGED; FEMALE; HUMANS; MALE; MIDDLE AGED; NORTH AMERICA; PARKINSON DISEASE; POINT MUTATION; PROTEIN-SERINE-THREONINE KINASES;

EID: 20444414834     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.20510     Document Type: Letter

References (5)

1. Shen J. Protein kinases linked to the pathogenesis of Parkinson's disease. Neuron 2004;44:575-577.
2. Valente EM, Abou-Sleiman PM, Caputo V, et al. Hereditary early-onset Parkinson's disease caused by mutations in PINK1. Science 2004;304:1158-1160.
3. Paisan-Ruiz C, Jain S, Evans EW, et al. Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease. Neuron 2004;44:595-600.
4. Hernandez DG, Paisan-Ruiz C, McInerney-Leo A, et al. Clinical and positron emission tomography of Parkinson's disease caused by LRRK2. Ann Neurol 2005;57:453-456.
5. Gelb DJ, Oliver E, Gilman S. Diagnostic criteria for Parkinson's disease. Arch Neurol 1999;56:33-39.