A dyslexia-associated variant in DCDC2 changes gene expression

Behavior Genetics

Volumn 41, Issue 1, 2011, Pages 58-66

  Meng, Haiying ^a   Powers, Natalie R ^a   Tang, Ling ^a   Cope, Natalie A ^a   Zhang, Ping Xia ^a   Fuleihan, Ramsay ^b   Gibson, Christopher ^a   Page, Grier P ^c   Gruen, Jeffrey R ^a  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b NORTHWESTERN UNIVERSITY   (United States)

^c RTI INTERNATIONAL   (United States)

Author keywords

Association; DCDC2; Dyslexia; Reading disability; Regulatory region

Indexed keywords

LUCIFERASE; NUCLEAR PROTEIN;

ALLELE; ARTICLE; BRAIN TISSUE; CONTROLLED STUDY; DOUBLECORTIN DOMAIN CONTAINING 2 GENE; DYSLEXIA; ENHANCER REGION; GEL MOBILITY SHIFT ASSAY; GENE; GENE DELETION; GENE EXPRESSION; GENE FUNCTION; GENE IDENTIFICATION; GENETIC ASSOCIATION; GENETIC CONSERVATION; GENETIC VARIABILITY; HUMAN; HUMAN TISSUE; OLIGONUCLEOTIDE PROBE; PROTEIN BINDING; RAJI CELL; REGULATORY SEQUENCE; REPORTER GENE; SHORT TANDEM REPEAT;

ALLELES; BRAIN; CELL LINE; CHROMOSOME DELETION; DYSLEXIA; ELECTROPHORETIC MOBILITY SHIFT ASSAY; ENHANCER ELEMENTS, GENETIC; GENE EXPRESSION; GENETIC LINKAGE; GENETIC VARIATION; HUMANS; INTRONS; MICROSATELLITE REPEATS; MICROTUBULE-ASSOCIATED PROTEINS; OLIGONUCLEOTIDE PROBES; REGULATORY SEQUENCES, NUCLEIC ACID;

EID: 79952443927     PISSN: 00018244     EISSN: 15733297     Source Type: Journal    
DOI: 10.1007/s10519-010-9408-3     Document Type: Article

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