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Volumn 99, Issue 6, 2002, Pages 3717-3722
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Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia
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Author keywords
[No Author keywords available]
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Indexed keywords
ADULT;
ARTICLE;
CHROMOSOME 22Q;
CHROMOSOME DELETION;
CLINICAL ARTICLE;
CONTROLLED STUDY;
DISEASE SEVERITY;
ENZYME SYNTHESIS;
FEMALE;
GENE LOCATION;
GENE LOCUS;
GENE SEQUENCE;
GENETIC LINKAGE;
GENETIC SUSCEPTIBILITY;
GENETIC VARIABILITY;
HUMAN;
ONSET AGE;
PRIORITY JOURNAL;
PSEUDOGENE;
SCHIZOIDISM;
SCHIZOPHRENIA;
AFRICA;
AGE OF ONSET;
ALLELES;
AMINO ACID SEQUENCE;
CHILD;
CHROMOSOMES, HUMAN, PAIR 22;
COHORT STUDIES;
EUROPE;
EXTRACELLULAR MATRIX PROTEINS;
GENETIC PREDISPOSITION TO DISEASE;
HAPLOTYPES;
HUMANS;
HYBRID CELLS;
LINKAGE DISEQUILIBRIUM;
MOLECULAR SEQUENCE DATA;
MUTATION;
MUTATION, MISSENSE;
PHENOTYPE;
POLYMORPHISM, SINGLE NUCLEOTIDE;
PROLINE OXIDASE;
PROTEINS;
PSEUDOGENES;
SCHIZOPHRENIA;
SEQUENCE ALIGNMENT;
UNITED STATES;
VARIATION (GENETICS);
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EID: 0842326677
PISSN: 00278424
EISSN: None
Source Type: Journal
DOI: 10.1073/pnas.042700699 Document Type: Article |
Times cited : (287)
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References (28)
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