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Volumn 7, Issue 1, 2002, Pages 67-71
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Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorder
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Author keywords
Association; Autistic disorder; Endophenotype; Linkage disequilibrium; Serotonin; Serotonin transporter
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Indexed keywords
SEROTONIN;
SEROTONIN TRANSPORTER;
ADOLESCENT;
ADULT;
ALLELE;
ARTICLE;
AUTISM;
CHILD;
CONTROLLED STUDY;
DISEASE PREDISPOSITION;
DNA FLANKING REGION;
FAMILY STUDY;
FEMALE;
GENE LINKAGE DISEQUILIBRIUM;
GENE LOCUS;
GENETIC ANALYSIS;
GENETIC ASSOCIATION;
GENETIC POLYMORPHISM;
GENETIC SUSCEPTIBILITY;
HUMAN;
INTRON;
MAJOR CLINICAL STUDY;
MALE;
PATHOGENESIS;
PHENOTYPE;
PRIORITY JOURNAL;
PROMOTER REGION;
REGULATOR GENE;
SEROTONIN BLOOD LEVEL;
VARIABLE NUMBER OF TANDEM REPEAT;
ADOLESCENT;
ADULT;
ALLELES;
AUTISTIC DISORDER;
BLOOD PLATELETS;
CARRIER PROTEINS;
CHILD;
CHILD, PRESCHOOL;
FEMALE;
GENETIC HETEROGENEITY;
GENETIC PREDISPOSITION TO DISEASE;
HAPLOTYPES;
HUMANS;
INTRONS;
LINKAGE DISEQUILIBRIUM;
MALE;
MEMBRANE GLYCOPROTEINS;
MEMBRANE TRANSPORT PROTEINS;
MINISATELLITE REPEATS;
MUTAGENESIS, INSERTIONAL;
NERVE TISSUE PROTEINS;
POLYMORPHISM, GENETIC;
RISK FACTORS;
SEQUENCE DELETION;
SEROTONIN;
SEROTONIN PLASMA MEMBRANE TRANSPORT PROTEINS;
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EID: 85047695651
PISSN: 13594184
EISSN: None
Source Type: Journal
DOI: 10.1038/sj.mp.4000923 Document Type: Article |
Times cited : (114)
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References (30)
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