Parkinson's disease: What remains of the "missing heritability"?

Movement Disorders

Volumn 26, Issue 11, 2011, Pages 1971-1973

  Pihlstrøm, Lasse ^a   Toft, Mathias ^a  

^a OSLO UNIVERSITY HOSPITAL   (Norway)

Author keywords

[No Author keywords available]

Indexed keywords

HLA DR ANTIGEN; LEUCINE RICH REPEAT KINASE 2;

ALLELE; ATTRIBUTABLE RISK; DISEASE PREDISPOSITION; EXOME; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENETIC ASSOCIATION; GENOTYPE; HERITABILITY; HUMAN; NOTE; PARKINSON DISEASE; PATHOGENESIS; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; HUMANS; PARKINSON DISEASE;

EID: 80052970270     PISSN: 08853185     EISSN: 15318257     Source Type: Journal    
DOI: 10.1002/mds.23898     Document Type: Note

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