SNP variations in the 7q33 region containing DGKI are associated with dyslexia in the Finnish and German populations

Behavior Genetics

Volumn 41, Issue 1, 2011, Pages 134-140

  Matsson, Hans ^a   Tammimies, Kristiina ^a   Zucchelli, Marco ^a   Anthoni, Heidi ^a   Onkamo, Päivi ^b   Nopola Hemmi, Jaana ^c   Lyytinen, Heikki ^d   Leppanen, Paavo H T ^d   Neuhoff, Nina ^e   Warnke, Andreas ^f   Schulte Körne, Gert ^e   Schumacher, Johannes ^g   Nöthen, Markus M ^g   Kere, Juha ^a,b   Peyrard Janvid, Myriam ^a  

^a KAROLINSKA INSTITUTE   (Sweden)

^b UNIVERSITY OF HELSINKI   (Finland)

^c HELSINKI UNIVERSITY CENTRAL HOSPITAL   (Finland)

^d UNIVERSITY OF JYVÄSKYLÄ   (Finland)

^e UNIVERSITY OF MUNICH   (Germany)

^f UNIVERSITY OF WÜRZBURG   (Germany)

^g UNIVERSITY OF BONN   (Germany)

Author keywords

Association; Fine mapping; Linkage; PDT; Reading disability; TDT

Indexed keywords

DIACYLGLYCEROL KINASE; DIACYLGLYCEROL KINASE IOTA; UNCLASSIFIED DRUG;

ARTICLE; CHROMOSOME 7Q; COHORT ANALYSIS; DGKI GENE; DYSLEXIA; FINLAND; GENE; GENE MAPPING; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC VARIABILITY; GERMANY; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; RISK FACTOR; SINGLE NUCLEOTIDE POLYMORPHISM;

ALLELES; CHILD; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 7; COHORT STUDIES; DIACYLGLYCEROL KINASE; DYSLEXIA; FEMALE; FINLAND; GENETIC ASSOCIATION STUDIES; GENETIC MARKERS; GENETIC VARIATION; GENETICS, POPULATION; GENOTYPE; GERMANY; HAPLOTYPES; HUMANS; LONGITUDINAL STUDIES; MALE; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 79952448889     PISSN: 00018244     EISSN: 15733297     Source Type: Journal    
DOI: 10.1007/s10519-010-9431-4     Document Type: Article

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