Genetic comorbidities in parkinson's disease

Human Molecular Genetics

Volumn 23, Issue 3, 2014, Pages 831-841

  Nalls, Mike A ^a   Saad, Mohamad ^b,c   Noyce, Alastair J ^d   Keller, Margaux F ^a,f   Schrag, Anette ^e   Bestwick, Jonathan P ^g   Traynor, Bryan J ^a   Raphael Gibbs, J ^a,e   Hernandez, Dena G ^a,e   Cookson, Mark R ^a   Morris, Huw R ^e,h   Williams, Nigel ^h   Gasser, Thomas ^i,j   Heutink, Peter ^j   Wood, Nick ^e,k   Hardy, John ^e   Martinez, Maria ^b,c   Singleton, Andrew B ^a  

^a NATIONAL INSTITUTE ON AGING   (United States)

^b INSERM   (France)

^c UNIVERSITÉ PAUL SABATIER   (France)

^d UNIVERSITY COLLEGE LONDON   (United Kingdom)

^e UNIVERSITY COLLEGE LONDON   (United Kingdom)

^f TEMPLE UNIVERSITY   (United States)

^g QUEEN MARY UNIVERSITY OF LONDON   (United Kingdom)

^h CARDIFF UNIVERSITY SCHOOL OF MEDICINE   (United Kingdom)

ⁱ UNIVERSITY OF TÜBINGEN   (Germany)

^j GERMAN CENTER FOR NEURODEGENERATIVE DISEASES DZNE   (Germany)

^k UNIVERSITY COLLEGE LONDON   (United Kingdom)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BRAIN TISSUE; COMORBIDITY; CROHN DISEASE; DISEASE ASSOCIATION; EPIDEMIOLOGICAL DATA; GENE EXPRESSION; GENE LOCUS; GENETIC ASSOCIATION; GENETIC RISK; GENOTYPE; HUMAN; METHYLATION; PARKINSON DISEASE; PHENOTYPE; PRIORITY JOURNAL; QUANTITATIVE TRAIT; SCHIZOPHRENIA; SINGLE NUCLEOTIDE POLYMORPHISM; SYSTEMATIC REVIEW;

COMORBIDITY; CPG ISLANDS; CROHN DISEASE; DNA METHYLATION; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; HUMANS; PARKINSON DISEASE; POLYMORPHISM, SINGLE NUCLEOTIDE; RISK FACTORS; SCHIZOPHRENIA;

EID: 84892453822     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddt465     Document Type: Article

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