Association of a rare variant with mismatch negativity in a region between KIAA0319 and DCDC2 in dyslexia

Behavior Genetics

Volumn 41, Issue 1, 2011, Pages 110-119

  Czamara, Darina ^a   Bruder, Jennifer ^b   Becker, Jessica ^c   Bartling, Jürgen ^b   Hoffmann, Per ^c   Ludwig, Kerstin Urte ^c   Müller Myhsok, Bertram ^a   Schulte Körne, Gerd ^b  

^a MAX PLANCK INSTITUTE OF PSYCHIATRY   (Germany)

^b UNIVERSITY OF MUNICH   (Germany)

^c UNIVERSITY OF BONN   (Germany)

Author keywords

Dyslexia; Imputing; Mismatch negativity; Rare variants; Speech perception

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; CHROMOSOME 6; DCDC2 GENE; DYSLEXIA; FEMALE; GENE; GENE LINKAGE DISEQUILIBRIUM; GENE LOCATION; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE; HUMAN; KIAA0319 GENE; MAJOR CLINICAL STUDY; MALE; MISMATCH NEGATIVITY; NUCLEOTIDE SEQUENCE; SCHOOL CHILD;

ADOLESCENT; ALLELES; CEREBRAL CORTEX; CHILD; CHROMOSOMES, HUMAN, PAIR 6; DNA MISMATCH REPAIR; DYSLEXIA; ELECTROENCEPHALOGRAPHY; EVOKED POTENTIALS; FEMALE; GENETIC VARIATION; GENOTYPE; HUMANS; MALE; MICROTUBULE-ASSOCIATED PROTEINS; NERVE TISSUE PROTEINS; POLYMORPHISM, SINGLE NUCLEOTIDE; SIGNAL PROCESSING, COMPUTER-ASSISTED; SPEECH PERCEPTION;

EID: 79952437992     PISSN: 00018244     EISSN: 15733297     Source Type: Journal    
DOI: 10.1007/s10519-010-9413-6     Document Type: Article

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