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Volumn 7, Issue 7, 2002, Pages 795-800
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Serotonin transporter gene promoter variants do not explain the hyperserotoninemia in autistic children
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Author keywords
Allelic association; Autism; Haplotype relative risk; Linkage disequilibrium; Peptiduria; Pervasive developmental disorders; Platelets; Serotoninemia; Transmission disequilibrium test
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Indexed keywords
SEROTONIN;
SEROTONIN TRANSPORTER;
ALLELE;
ANALYSIS OF VARIANCE;
ARTICLE;
AUTISM;
CHILD;
CONTROLLED STUDY;
CORRELATION ANALYSIS;
GENETIC ASSOCIATION;
GENETIC POLYMORPHISM;
GENETIC VARIABILITY;
GENOTYPE;
HUMAN;
INHERITANCE;
MAJOR CLINICAL STUDY;
PRIORITY JOURNAL;
PROBABILITY;
PROMOTER REGION;
QUANTITATIVE ANALYSIS;
RELATIVE;
SEROTONIN BLOOD LEVEL;
AUTISTIC DISORDER;
CARRIER PROTEINS;
CHILD;
FAMILY HEALTH;
FEMALE;
HAPLOTYPES;
HUMANS;
LINKAGE DISEQUILIBRIUM;
MALE;
MEMBRANE GLYCOPROTEINS;
MEMBRANE TRANSPORT PROTEINS;
NERVE TISSUE PROTEINS;
PROMOTER REGIONS (GENETICS);
SEROTONIN;
SEROTONIN PLASMA MEMBRANE TRANSPORT PROTEINS;
VARIATION (GENETICS);
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EID: 0036373349
PISSN: 13594184
EISSN: None
Source Type: Journal
DOI: 10.1038/sj.mp.4001069 Document Type: Article |
Times cited : (49)
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References (30)
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