DJ-1: The second gene for early onset Parkinson disease

Neurology

Volumn 62, Issue 3, 2004, Pages 357-358

  Bandmann, Oliver ^a  

^a UNIVERSITY OF SHEFFIELD   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

L166P PROTEIN; LEVODOPA; PROTEIN; UNCLASSIFIED DRUG;

ALLELIC EXCLUSION; ALPHA SYNUCLEIN GENE; AUTOSOMAL RECESSIVE DISORDER; CLINICAL FEATURE; DJ 1 GENE; EDITORIAL; FAMILIAL DISEASE; GENE; GENE MUTATION; GENE SEQUENCE; GENETIC POLYMORPHISM; GENETIC RISK; GENETIC SUSCEPTIBILITY; HEREDITY; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; LEWY BODY; ONSET AGE; PARK6 GENE; PARK7 GENE; PARKIN GENE; PARKINSON DISEASE; POINT MUTATION; POPULATION GENETICS; POSITRON EMISSION TOMOGRAPHY; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN AGGREGATION; RNA SPLICING;

EID: 1042288165     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.62.3.357     Document Type: Editorial

References (10)

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9. Macedo MG, Anar B, Bronner IF, et al. The DJ-1L166P mutant protein associated with early onset Parkinson's disease is unstable and forms higher-order protein complexes. Hum Mol Genet 2003;12: 2807-2816.
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