An association study of sequence variants in the forkhead box P2 (FOXP2) gene and adulthood attention-deficit/hyperactivity disorder in two European samples

Psychiatric Genetics

Volumn 22, Issue 4, 2012, Pages 155-160

  Ribasés, Marta ^a   Sánchez Mora, Cristina ^a   Ramos Quiroga, Josep Antoni ^a,c   Bosch, Rosa ^a,c   Gómez, Núria ^a   Nogueira, Mariana ^a   Corrales, Montse ^a   Palomar, Gloria ^a   Jacob, Christian P ^d   Gross Lesch, Silke ^d   Kreiker, Susanne ^d   Reif, Andreas ^d   Lesch, Klaus Peter ^d   Cormand, Bru ^a,b   Casas, Miquel ^a,c   Bayés, Mónica ^a  

^a UNIVERSITY OF BARCELONA   (Spain)

^b CENTRO DE INVESTIGACIÓN BIOMÉDICA EN RED DE ENFERMEDADES RARAS CIBERER   (Spain)

^c UNIVERSITAT AUTÒNOMA DE BARCELONA   (Spain)

^d UNIVERSITY OF WÜRZBURG   (Germany)

Author keywords

attention deficit hyperactivity disorder; case control association study; forkhead box P2; learning disability; single nucleotide polymorphism

Indexed keywords

TRANSCRIPTION FACTOR FOXP2;

ADULT; ARTICLE; ATTENTION DEFICIT DISORDER; CASE CONTROL STUDY; CONTROLLED STUDY; GENE SEQUENCE; GENETIC ASSOCIATION; GERMANY; HUMAN; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

ADULT; ATTENTION DEFICIT DISORDER WITH HYPERACTIVITY; CASE-CONTROL STUDIES; EUROPEAN CONTINENTAL ANCESTRY GROUP; FORKHEAD TRANSCRIPTION FACTORS; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; GERMANY; HAPLOTYPES; HUMANS; POLYMORPHISM, SINGLE NUCLEOTIDE; SOFTWARE;

EID: 84863483501     PISSN: 09558829     EISSN: 14735873     Source Type: Journal    
DOI: 10.1097/YPG.0b013e328353957e     Document Type: Article

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