Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia

American Journal of Human Genetics

Volumn 78, Issue 1, 2006, Pages 52-62

  Schumacher, Johannes ^a   Anthoni, Heidi ^b   Dahdouh, Faten ^a   König, Inke R ^c   Hillmer, Axel M ^a   Kluck, Nadine ^a   Manthey, Malou ^a   Plume, Ellen ^d   Warnke, Andreas ^d   Remschmidt, Helmut ^e   Hülsmann, Jutta ^e   Cichon, Sven ^a   Lindgren, Cecilia M ^b   Propping, Peter ^a   Zucchelli, Marco ^b   Ziegler, Andreas ^c   Peyrard Janvid, Myriam ^b   Schulte Körne, Gerd ^e   Nöthen, Markus M ^a   Kere, Juha ^b,f  

^a UNIVERSITY OF BONN   (Germany)

^b KAROLINSKA INSTITUTE   (Sweden)

^c UNIVERSITY HOSPITAL SCHLESWIG HOLSTEIN   (Germany)

^d UNIVERSITY OF WÜRZBURG   (Germany)

^e PHILIPPS UNIVERSITY MARBURG   (Germany)

^f UNIVERSITY OF HELSINKI   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

DOUBLECORTIN; GENE PRODUCT; PROTEIN DCDC2; UNCLASSIFIED DRUG;

ADULT; ARTICLE; CELL MATURATION; CELL MIGRATION; CHILD; CHROMOSOME 6P; DCDC2 GENE; DISEASE SEVERITY; DYSLEXIA; FETUS; GENE; GENE CLUSTER; GENE EXPRESSION; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENETIC MARKER; GENETIC SUSCEPTIBILITY; GERMANY; HAPLOTYPE; HUMAN; KAAG1 GENE; NERVE CELL; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN FUNCTION; SEQUENCE HOMOLOGY; VMP GENE;

EID: 29244468273     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/498992     Document Type: Article

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