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Volumn 35, Issue 3, 2010, Pages 656-664

Multicenter analysis of the SLC6A3/DAT1 VNTR haplotype in persistent ADHD suggests differential involvement of the gene in childhood and persistent ADHD

(33)  Franke, Barbara a,b   Vasquez, Alejandro Arias a,b   Johansson, Stefan c,d   Hoogman, Martine b   Romanos, Jasmin e   Boreatti Hümmer, Andrea e   Heine, Monika e   Jacob, Christian P e   Lesch, Klaus Peter e   Casas, Miguel f,g   Ribasés, Marta f   Bosch, Rosa f   Sánchez Mora, Cristina f   Gómez Barros, Nria f   Fernndez Castillo, Noèlia h   Bayés, Mònica i,j,k   Halmøy, Anne c   Halleland, Helene c   Landaas, Elisabeth T c,d   Fasmer, Ole B c,d   more..


Author keywords

Dopamine; Neurogenetics; Psychiatry and behavioral sciences; Transporters

Indexed keywords

ALLELE; ARTICLE; ATTENTION DEFICIT DISORDER; DAT1 GENE; GENE; GENOTYPE; HAPLOTYPE; HUMAN; INTRON; MENTAL DISEASE; PRIORITY JOURNAL; RISK FACTOR; SLC6A3 GENE; VARIABLE NUMBER OF TANDEM REPEAT;

EID: 75749145001     PISSN: 0893133X     EISSN: None     Source Type: Journal    
DOI: 10.1038/npp.2009.170     Document Type: Article
Times cited : (155)

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