Lack of support for association between the copy number variants in the FCGR locus and schizophrenia: A case control study

Neuroscience Letters

Volumn 522, Issue 2, 2012, Pages 85-91

  Zhao, Arman ^a   Xiang, Yuqian ^a   Xu, Jiawei ^a   Li, Qiaoli ^a   Wang, Lei ^a   Xing, Qinghe ^a   Zhang, Zhou ^b   Liu, Yun ^a   Feng, Guoyin ^d   He, Lin ^a,b,c   Zhao, Xinzhi ^a  

^a FUDAN UNIVERSITY   (China)

^b Chinese Academy of Sciences   (China)

^c SHANGHAI JIAO TONG UNIVERSITY   (China)

^d SHANGHAI MENTAL HEALTH CENTER   (China)

Author keywords

Chinese Han ancestry; CNV based association studies; FCGR locus; Multiallelic CNVs; Schizophrenia

Indexed keywords

FCGR PROTEIN; PROTEIN; UNCLASSIFIED DRUG;

ADULT; ARTICLE; ASSAY; CASE CONTROL STUDY; COHORT ANALYSIS; CONTROLLED STUDY; COPY NUMBER VARIATION; DIPLOIDY; DISEASE ASSOCIATION; FEMALE; GENE DELETION; GENE LOCUS; GENOME; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; REGULATORY SEQUENCE; SCHIZOPHRENIA;

ASIAN CONTINENTAL ANCESTRY GROUP; CASE-CONTROL STUDIES; GENE DOSAGE; GENETIC ASSOCIATION STUDIES; GENETIC LOCI; GENETIC PREDISPOSITION TO DISEASE; HUMANS; RECEPTORS, IGG; SCHIZOPHRENIA;

EID: 84863863804     PISSN: 03043940     EISSN: 18727972     Source Type: Journal    
DOI: 10.1016/j.neulet.2012.04.037     Document Type: Article

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