SCOPUS 정보 검색 플랫폼

Volumn 7, Issue 1, 2002, Pages 67-71

Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorder

(16) Betancur, C a Corbex, M b Spielewoy, C a Philippe, A a,c Laplanche, J L a,d Launay, J M d Gillberg, C e Mouren Simeoni M C f Hamon, M a Giros, B a Nosten Bertrand, M a Leboyer, M a,c Gillberg, Christopher e Rastam, Maria e Gillberg, Carina e Nydén, Agneta e

a INSERM (France)

b PITIÉ SALPÊTRIÈRE HOSPITAL (France)

c HENRI MONDOR HOSPITAL (France)

d HÔPITAL LARIBOISIÈRE (France)

e UNIVERSITY OF GOTHENBURG (Sweden)

f HÔPITAL ROBERT DEBRÉ (France)

Author keywords

Association; Autistic disorder; Endophenotype; Linkage disequilibrium; Serotonin; Serotonin transporter

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;

EID: 85047695651 PISSN: 13594184 EISSN: None Source Type: Journal
DOI: 10.1038/sj.mp.4000923 Document Type: Article

Times cited : (113)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.