Hyperserotonemia in Autism: The potential role of 5HT-related gene variants

Collegium Antropologicum

Volumn 32, Issue SUPPL. 1, 2008, Pages 75-80

  Hranilović, Dubravka ^a   Novak, Ruder ^b   Babić, Marina ^c   Novokmet, Mislav ^a   Bujas Petković, Zoraná ^d   Jernej, Branimir ^e  

^a UNIVERSITY OF ZAGREB   (Croatia)

^b UNIVERSITY OF ZAGREB   (Croatia)

^c UNIVERSITY OF RIJEKA   (Croatia)

^d Psychiatric Hospitalfor children and adolescents   (Croatia)

^e RUDER BO KOVI INSTITUTE   (Croatia)

Author keywords

5HT2A receptor; Autism; Hyperserotonemia; Monoamine oxydase A; Serotonin transporter; Tryptophan hydroxylase

Indexed keywords

AMINE OXIDASE (FLAVIN CONTAINING); SEROTONIN; SEROTONIN 2 RECEPTOR; SEROTONIN TRANSPORTER; TRYPTOPHAN HYDROXYLASE;

ADOLESCENT; ADULT; AUTISM; BIOSYNTHESIS; BLOOD; CHILD; CLINICAL TRIAL; CONFERENCE PAPER; FEMALE; GENETIC POLYMORPHISM; GENETICS; GENOTYPE; HUMAN; MALE; METABOLISM; PHYSIOLOGY; PRESCHOOL CHILD;

ADOLESCENT; ADULT; AUTISTIC DISORDER; CHILD; CHILD, PRESCHOOL; FEMALE; GENOTYPE; HUMANS; MALE; MONOAMINE OXIDASE; POLYMORPHISM, GENETIC; RECEPTORS, SEROTONIN, 5-HT2; SEROTONIN; SEROTONIN PLASMA MEMBRANE TRANSPORT PROTEINS; TRYPTOPHAN HYDROXYLASE;

EID: 39449130477     PISSN: 03506134     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper

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