PLA2G6 mutations and Parkinson's disease

Annals of Neurology

Volumn 67, Issue 1, 2010, Pages 148-

  Tan, E K ^a,b,c   Ho, P ^a   Tan, L ^b   Prakash, K M ^a,b   Zhao, Y ^a  

^a SINGAPORE GENERAL HOSPITAL   (Singapore)

^b NATIONAL NEUROSCIENCE INSTITUTE   (Singapore)

^c DUKE NUS MEDICAL SCHOOL   (Singapore)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; PROLINE;

ATP13A2 GENE; COMPUTER ASSISTED TOMOGRAPHY; DISEASE COURSE; DYSTONIA; FAMILY HISTORY; GENE; GENE MUTATION; HUMAN; LETTER; NEUROAXONAL DYSTROPHY; NUCLEAR MAGNETIC RESONANCE IMAGING; PARKINSON DISEASE; PHENOTYPE; PLG2G6 GENE; PRIORITY JOURNAL;

AGED; BRAIN; COHORT STUDIES; DYSTONIA; GROUP VI PHOSPHOLIPASES A2; HUMANS; MALE; MUTATION, MISSENSE; PARKINSON DISEASE; POINT MUTATION; SEQUENCE ANALYSIS, DNA; TOMOGRAPHY, X-RAY COMPUTED;

EID: 77649316334     PISSN: 03645134     EISSN: 15318249     Source Type: Journal    
DOI: 10.1002/ana.21663     Document Type: Letter

References (3)

1. Paisan-Ruiz C, Bhatia KP, Li A, et al. Characterization of PLA2G6 as a locus for dystonia-parkinsonism. Ann Neurol (in press).
2. Di Fonzo A, Chien HF, Socal M, et al. ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease. Neurology 2007;68:1557-1562.
3. Lin CH, Tan EK, Chen ML, et al. Novel ATP13A2 variant associated with Parkinson disease in Taiwan and Singapore. Neurology 2008;71:1727-1732.