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Volumn 6, Issue 8, 2011, Pages

Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a Northern Swedish population

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; ATF5 GENE; CONTROLLED STUDY; DISC1 GENE; FEMALE; FEZ1 GENE; GENE; GENE INTERACTION; GENE SEQUENCE; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GRB2 GENE; HUMAN; LIS 1 GENE; MAJOR CLINICAL STUDY; MALE; MENTAL DISEASE; MISSENSE MUTATION; MUTATIONAL ANALYSIS; NDE1 GENE; NDEL1 GENE; ONSET AGE; PATHOGENESIS; PDE4B GENE; SCHIZOPHRENIA; SWEDEN; TRAF3IP1 GENE; YWHAE GENE; ZNF365 GENE; BIOLOGY; CASE CONTROL STUDY; DNA SEQUENCE; FRAMESHIFT MUTATION; GENE FREQUENCY; GENETIC PREDISPOSITION; GENETICS; METHODOLOGY; MIDDLE AGED; NUCLEOTIDE SEQUENCE; POPULATION GENETICS; REPRODUCIBILITY; SIGNAL TRANSDUCTION;

EID: 80051617030     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0023450     Document Type: Article
Times cited : (42)

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