Genetic variant in KIAA0319, but not in DYX1C1, is associated with risk of dyslexia: An integrated meta-analysis

American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics

Volumn 159 B, Issue 8, 2012, Pages 970-976

  Zou, Li ^a   Chen, Wei ^a   Shao, Shanshan ^a   Sun, Zhao ^a   Zhong, Rong ^a   Shi, Junxin ^a   Miao, Xiaoping ^a   Song, Ranran ^a  

^a HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

Author keywords

Dyslexia; DYX1C1; KIAA0319; Meta analysis; Susceptibility

Indexed keywords

CYTOSINE; THYMINE;

ALLELE; ARTICLE; CASE CONTROL STUDY; CONFIDENCE INTERVAL; CONTROLLED STUDY; DATA ANALYSIS; DATA ANALYSIS SOFTWARE; DNA POLYMORPHISM; DYSLEXIA; DYX1C1 GENE; GENE; GENETIC ASSOCIATION; GENETIC HETEROGENEITY; GENETIC PROCEDURES; GENETIC RISK; GENETIC VARIABILITY; HUMAN; KIAA0319 GENE; PRIORITY JOURNAL; RISK; SENSITIVITY ANALYSIS; STRATIFIED SAMPLE; TRANSMISSION DISEQUILIBRIUM TEST;

CASE-CONTROL STUDIES; DYSLEXIA; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; HUMANS; NERVE TISSUE PROTEINS; NUCLEAR PROTEINS; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 84869072315     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/ajmg.b.32102     Document Type: Article

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