Association of reading disabilities with regions marked by acetylated H3 histones in KIAA0319

American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics

Volumn 153, Issue 2, 2010, Pages 447-462

  Couto, Jillian M ^a,c   Livne Bar, Izzy ^a   Huang, Katherine ^a   Xu, Zhaodong ^a   Cate Carter, Tasha ^b   Feng, Yu ^a   Wigg, Karen ^a   Humphries, Tom ^b   Tannock, Rosemary ^b   Kerr, Elizabeth N ^b   Lovett, Maureen W ^b   Bremner, Rod ^a   Barr, Cathy L ^a,b  

^a UNIVERSITY HEALTH NETWORK   (Canada)

^b HOSPITAL FOR SICK CHILDREN   (Canada)

^c UNIVERSITY OF GLASGOW   (United Kingdom)

Author keywords

6p; Association; ChIP chip; Dyslexia; Reading disabilities

Indexed keywords

HISTONE; MOLECULAR MARKER;

ACETYLATION; ALLELE; ARTICLE; CHROMATIN IMMUNOPRECIPITATION; CHROMOSOME 6P; DYSLEXIA; GENE CONTROL; GENE LOCUS; GENE MAPPING; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOME; HAPLOTYPE; HUMAN; INTRON; MARKER GENE; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL;

3' UNTRANSLATED REGIONS; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 6; DYSLEXIA; FAMILY HEALTH; GENETIC MARKERS; GENETIC VARIATION; HAPLOTYPES; HISTONES; HUMANS; IMMUNOPRECIPITATION; LINKAGE DISEQUILIBRIUM; NERVE TISSUE PROTEINS; POLYMORPHISM, SINGLE NUCLEOTIDE; PROMOTER REGIONS, GENETIC;

EID: 77349092836     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/ajmg.b.30999     Document Type: Article

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