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Volumn 99, Issue 8, 2002, Pages 4755-4756
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A compelling genetic hypothesis for a complex disease: PRODH2/DGCR6 variation leads to schizophrenia susceptibility
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Author keywords
[No Author keywords available]
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Indexed keywords
PROLINE;
PROLINE DEHYDROGENASE;
PYRROLINE DERIVATIVE;
AUTOSOMAL DOMINANT INHERITANCE;
AUTOSOMAL RECESSIVE INHERITANCE;
CHROMOSOME 22Q;
DISEASE PREDISPOSITION;
GENE DELETION;
GENE DUPLICATION;
GENE EXPRESSION;
GENE FREQUENCY;
GENE FUNCTION;
GENE IDENTIFICATION;
GENE MAPPING;
GENE MUTATION;
GENE SEQUENCE;
GENE STRUCTURE;
GENETIC SUSCEPTIBILITY;
GENETIC VARIABILITY;
HUMAN;
NONHUMAN;
NOTE;
ONSET AGE;
PATHOPHYSIOLOGY;
PRIORITY JOURNAL;
PSEUDOGENE;
SCHIZOPHRENIA;
SINGLE NUCLEOTIDE POLYMORPHISM;
ANIMALS;
CHROMOSOMES, HUMAN, PAIR 22;
EXTRACELLULAR MATRIX PROTEINS;
GENETIC PREDISPOSITION TO DISEASE;
HUMANS;
MICE;
POLYMORPHISM, GENETIC;
PROLINE OXIDASE;
PROTEINS;
SCHIZOPHRENIA;
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EID: 0037117578
PISSN: 00278424
EISSN: None
Source Type: Journal
DOI: 10.1073/pnas.092158299 Document Type: Note |
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Times cited : (31)
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References (14)
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