A family- and population-based study of the UFD1L gene for schizophrenia

American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics

Volumn 147, Issue 7, 2008, Pages 1076-1079

  Xie, Lin ^a   Ye, Lin ^a   Ju, Guizhi ^a   Xu, Qi ^b   Zhang, Xuan ^a   Liu, Shuzheng ^a   Shi, Jieping ^a   Yu, Yaqin ^a   Wang, Zhenqi ^a   Shen, Yan ^b   Wei, Jun ^c  

^a JILIN UNIVERSITY   (China)

^b INSTITUTE OF BASIC MEDICAL SCIENCES   (China)

^c UNIVERSITY OF THE HIGHLANDS AND ISLANDS   (United Kingdom)

Author keywords

Chromosome 22; Schizophrenia; Single nucleotide polymorphisms (SNPs); UFD1L

Indexed keywords

ADULT; ARTICLE; CONTROLLED STUDY; DISEASE ASSOCIATION; FEMALE; GENE; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENETIC ASSOCIATION; GENOTYPE; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; SCHIZOPHRENIA; SINGLE NUCLEOTIDE POLYMORPHISM; UFDL1 GENE;

5' UNTRANSLATED REGIONS; ADOLESCENT; ADULT; ALLELES; ASIAN CONTINENTAL ANCESTRY GROUP; CASE-CONTROL STUDIES; CHINA; FAMILY HEALTH; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENETICS, POPULATION; HAPLOTYPES; HUMANS; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE; PROMOTER REGIONS (GENETICS); PROTEINS; SCHIZOPHRENIA;

EID: 55349093318     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/ajmg.b.30719     Document Type: Article

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