Identification of high risk DISC1 structural variants with a 2% attributable risk for schizophrenia

Biochemical and Biophysical Research Communications

Volumn 367, Issue 3, 2008, Pages 700-706

  Song, Wenjia ^a   Li, Wenyan ^a   Feng, Jinong ^a   Heston, Leonard L ^b   Scaringe, William A ^a   Sommer, Steve S ^a  

^a CITY OF HOPE NATIONAL MEDICAL CENTER   (United States)

^b UNIVERSITY OF WASHINGTON   (United States)

Author keywords

Case control study; Disrupted in schizophrenia 1 (DISC1) gene; Mutation detection; Schizophrenia

Indexed keywords

ARTICLE; ATTRIBUTABLE RISK; CAUCASIAN; CONTROLLED STUDY; DISC1 GENE; FEMALE; FRAMESHIFT MUTATION; GENE; GENE DISRUPTION; GENE FREQUENCY; GENE REPLICATION; GENE STRUCTURE; GENETIC RISK; GENETIC VARIABILITY; HAPLOTYPE MAP; HUMAN; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SCHIZOPHRENIA;

ADULT; ALLELES; CASE-CONTROL STUDIES; COHORT STUDIES; FEMALE; GENE FREQUENCY; HETEROZYGOTE; HUMANS; MALE; MINNESOTA; MUTATION, MISSENSE; NERVE TISSUE PROTEINS; ODDS RATIO; RISK ASSESSMENT; RISK FACTORS; SCHIZOPHRENIA;

EID: 38649101571     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2007.12.117     Document Type: Article

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