Identification of rare mutations of synaptogyrin 1 gene in patients with schizophrenia

Journal of Psychiatric Research

Volumn 41, Issue 12, 2007, Pages 1027-1031

  Cheng, Min Chih ^a   Chen, Chia Hsiang ^a,b  

^a TZU CHI UNIVERSITY   (Taiwan)

^b NATIONAL HEALTH RESEARCH INSTITUTES   (Taiwan)

Author keywords

Chromosome 22q; Etiology; Gene; Mutation; Schizophrenia; Synaptogyrin 1

Indexed keywords

ADULT; ARTICLE; CASE CONTROL STUDY; CODON; COHORT ANALYSIS; COMPUTER PROGRAM; FEMALE; FRAMESHIFT MUTATION; GENE; GENE LINKAGE DISEQUILIBRIUM; GENE MUTATION; GENETIC ASSOCIATION; HAPLOTYPE; HUMAN; INTRON; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; PREDICTION; PRIORITY JOURNAL; PROMOTER REGION; SCHIZOPHRENIA; SINGLE NUCLEOTIDE POLYMORPHISM; SYNAPTOGYRIN 1 GENE; TAIWAN; TRANSCRIPTION INITIATION SITE;

ADULT; ASIAN CONTINENTAL ANCESTRY GROUP; CASE-CONTROL STUDIES; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MEMBRANE PROTEINS; MIDDLE AGED; MUTATION; NERVE TISSUE PROTEINS; SCHIZOPHRENIA;

EID: 34548130154     PISSN: 00223956     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpsychires.2006.08.010     Document Type: Article

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