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Volumn 105, Issue 6, 2001, Pages 529-533
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Association study of a promoter polymorphism of UFD1L gene with schizophrenia
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Author keywords
Chromosome 22; DiGeorge syndrome; Linkage analysis; Ubiquitin; VCFS
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Indexed keywords
HYBRID PROTEIN;
UBIQUITIN;
ADULT;
ARTICLE;
CHROMOSOME 22Q;
CHROMOSOME DELETION;
CLINICAL ARTICLE;
CONTROLLED STUDY;
DIGEORGE SYNDROME;
DNA FLANKING REGION;
EXON;
FEMALE;
GENE EXPRESSION;
GENE MAPPING;
GENETIC ASSOCIATION;
GENETIC SUSCEPTIBILITY;
HEMIZYGOSITY;
HUMAN;
MALE;
NUCLEOTIDE SEQUENCE;
PRIORITY JOURNAL;
PROMOTER REGION;
SCHIZOIDISM;
SCHIZOPHRENIA;
SINGLE NUCLEOTIDE POLYMORPHISM;
VELOCARDIOFACIAL SYNDROME;
ADULT;
ALLELES;
CANADA;
CELL LINE;
COHORT STUDIES;
DNA;
FEMALE;
GENE FREQUENCY;
GENOTYPE;
GREEN FLUORESCENT PROTEINS;
HUMANS;
ITALY;
LUMINESCENT PROTEINS;
MALE;
MIDDLE AGED;
POLYMORPHISM, GENETIC;
PROMOTER REGIONS (GENETICS);
PROTEINS;
RECOMBINANT FUSION PROTEINS;
SCHIZOPHRENIA;
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EID: 0035828111
PISSN: 15524841
EISSN: 1552485X
Source Type: Journal
DOI: 10.1002/ajmg.1489 Document Type: Article |
Times cited : (36)
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References (25)
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