Erratum: Imaging genetics of FOXP2 in dyslexia (European Journal of Human Genetics (2012) 20 (224-229) DOI: 10.1038/ejhg.2011.160);Imaging genetics of FOXP2 in dyslexia

European Journal of Human Genetics

Volumn 20, Issue 2, 2012, Pages 224-229

  Wilcke, Arndt ^a,b   Ligges, Carolin ^c   Burkhardt, Jana ^a   Alexander, Michael ^d   Wolf, Christiane ^e   Quente, Elfi ^a   Ahnert, Peter ^a   Hoffmann, Per ^d   Becker, Albert ^f   Müller Myhsok, Bertram ^f   Cichon, Sven ^d,g   Boltze, Johannes ^a,b   Kirsten, Holger ^a,b  

^a UNIVERSITY OF LEIPZIG   (Germany)

^b FRAUNHOFER INSTITUTE FOR CELL THERAPY AND IMMUNOLOGY   (Germany)

^c FRIEDRICH SCHILLER UNIVERSITY JENA   (Germany)

^d UNIVERSITY OF BONN   (Germany)

^e MAX PLANCK INSTITUTE OF PSYCHIATRY   (Germany)

^f UNIVERSITY HOSPITAL BONN   (Germany)

^g FORSCHUNGSZENTRUM JÜLICH   (Germany)

Author keywords

dyslexia; fMRI; FOXP2; imaging genetics

Indexed keywords

TRANSCRIPTION FACTOR FOXP2;

ARTICLE; BRAIN TISSUE; CASE CONTROL STUDY; CHILD; CONTROLLED STUDY; DYSLEXIA; FEMALE; FRONTAL LOBE; FUNCTIONAL MAGNETIC RESONANCE IMAGING; GENE EXPRESSION; GENE MUTATION; GENETIC ASSOCIATION; GENETIC RISK; HIPPOCAMPUS; HUMAN; HUMAN TISSUE; MAJOR CLINICAL STUDY; MALE; NEUROIMAGING; PARIETAL LOBE; PHONETICS; PRIORITY JOURNAL; RISK ASSESSMENT; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; TEMPORAL LOBE;

EID: 84855790585     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/ejhg.2012.31     Document Type: Erratum

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