Intronic rs2147363 variant in ATP7B transcription factor-binding site associated with Alzheimer's disease

Journal of Alzheimer's Disease

Volumn 37, Issue 2, 2013, Pages 453-459

  Bucossi, Serena ^a,b   Polimanti, Renato ^c   Ventriglia, Mariacarla ^a,b   Mariani, Stefania ^a,b   Siotto, Mariacristina ^d   Ursini, Francesca ^a   Trotta, Laura ^a   Scrascia, Federica ^a   Callea, Antonio ^a   Vernieri, Fabrizio ^a   Squitti, Rosanna ^b,e  

^a UNIVERSITY CAMPUS BIO MEDICO   (Italy)

^b IRCCS ISTITUTO CENTRO SAN GIOVANNI DI DIO FATEBENEFRATELLI   (Italy)

^c UNIVERSITY OF ROME TOR VERGATA   (Italy)

^d IRCCS FONDAZIONE DON CARLO GNOCCHI   (Italy)

^e IRCCS SAN RAFFAELE PISANA   (Italy)

Author keywords

Alzheimer's disease; ATP7B; cis regulatory element; copper; intronic variant

Indexed keywords

TRANSCRIPTION FACTOR;

AGED; ALZHEIMER DISEASE; ARTICLE; BINDING SITE; COMPUTER MODEL; CONTROLLED STUDY; FEMALE; GENE LINKAGE DISEQUILIBRIUM; GENE MUTATION; GENETIC ASSOCIATION; GENETIC RISK; GENETIC SCREENING; GENETIC VARIABILITY; HEREDITY; HUMAN; INTRON; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; REGULATORY SEQUENCE; SINGLE NUCLEOTIDE POLYMORPHISM; WILSON DISEASE;

ADENOSINE TRIPHOSPHATASES; AGED; AGED, 80 AND OVER; ALZHEIMER DISEASE; BINDING SITES; CATION TRANSPORT PROTEINS; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; INTRONS; LINKAGE DISEQUILIBRIUM; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 84883798909     PISSN: 13872877     EISSN: 18758908     Source Type: Journal    
DOI: 10.3233/JAD-130431     Document Type: Article

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