The genetics of reading disability in an often excluded sample: Novel loci suggested for reading disability in rolandic epilepsy

PLoS ONE

Volumn 7, Issue 7, 2012, Pages

  Strug, Lisa J ^a,b   Addis, Laura ^c   Chiang, Theodore ^a   Baskurt, Zeynep ^a   Li, Weili ^a   Clarke, Tara ^d   Hardison, Huntley ^e   Kugler, Steven L ^f   Mandelbaum, David E ^g   Novotny, Edward J ^h   Wolf, Steven M ⁱ   Pal, Deb K ^c,j  

^a HOSPITAL FOR SICK CHILDREN   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

^c KING'S COLLEGE LONDON   (United Kingdom)

^d Department of Medicine   (United States)

^e ST CHRISTOPHER'S HOSPITAL FOR CHILDREN   (United States)

^f UNIVERSITY OF PENNSYLVANIA   (United States)

^g BROWN UNIVERSITY   (United States)

^h YALE UNIVERSITY MEDICAL CENTER   (United States)

ⁱ BETH ISRAEL MEDICAL CENTER   (United States)

^j Department of Medicine   (United States)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHILD; CHROMOSOME 1Q; CHROMOSOME 7Q; CONTROLLED STUDY; DATA ANALYSIS; DISC1 GENE; DISEASE ASSOCIATION; DYSLEXIA; FAMILY STUDY; GENE; GENE LOCUS; GENE REPLICATION; GENETIC ASSOCIATION; GENETIC DATABASE; GENETIC LINKAGE; HUMAN; PEDIGREE ANALYSIS; PHENOTYPE; PRESCHOOL CHILD; ROLANDIC EPILEPSY; SCHOOL CHILD; SEMA3C GENE;

CANADA; CHROMOSOMES, HUMAN, PAIR 1; CHROMOSOMES, HUMAN, PAIR 7; DATABASES, GENETIC; DYSLEXIA; EPILEPSY, ROLANDIC; FEMALE; GENETIC LOCI; GENETIC PREDISPOSITION TO DISEASE; GENOME, HUMAN; HUMANS; LANGUAGE DISORDERS; LOD SCORE; MALE; NERVE TISSUE PROTEINS; PEDIGREE; REPRODUCIBILITY OF RESULTS; SEMAPHORINS; SEQUENCE ANALYSIS, DNA;

EID: 84864014047     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0040696     Document Type: Article

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