Deletion polymorphism in the coding region of the human NESP55 alternative transcript of GNAS1

Molecular and Cellular Probes

Volumn 14, Issue 3, 2000, Pages 191-194

  Kim, S J ^a   Gonen, D ^a   Hanna, G L ^b   Leventhal, B L ^a   Cook Jr , E H ^a  

^a UNIVERSITY OF CHICAGO   (United States)

^b UNIVERSITY OF MICHIGAN HEALTH SYSTEM   (United States)

Author keywords

GNAS1; LSAL; NESP55; Polymorphism; Serotonin; SNP

Indexed keywords

ARTICLE; ATTENTION DEFICIT DISORDER; AUTISM; COMPULSION; CONTROLLED STUDY; DNA POLYMORPHISM; GENE DELETION; GENE FREQUENCY; GENOTYPE; HUMAN; HYPERACTIVITY; MAJOR CLINICAL STUDY; NUCLEOTIDE SEQUENCE; OBSESSION; PHENOTYPE; PRIORITY JOURNAL; SEROTONINERGIC TRANSMISSION;

EID: 0343603576     PISSN: 08908508     EISSN: None     Source Type: Journal    
DOI: 10.1006/mcpr.2000.0300     Document Type: Article

References (10)

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