COMT Val158met genotype and striatal D2/3 receptor binding in adults with 22q11 deletion syndrome

Synapse

Volumn 65, Issue 9, 2011, Pages 967-970

  Boot, Erik ^a,b   Booij, Jan ^a   Zinkstok, Janneke R ^a   Baas, Frank ^a   Swillen, Ann ^c   Owen, Michael J ^d   Murphy, Declan G ^e   Murphy, Kieran C ^f   Linszen, Don H ^a   Van Amelsvoort, Thérèse A ^a  

^a UNIVERSITY OF AMSTERDAM   (Netherlands)

^b Ipse de Bruggen   (Netherlands)

^c UNIVERSITY OF LEUVEN   (Belgium)

^d CARDIFF UNIVERSITY   (United Kingdom)

^e KING'S COLLEGE LONDON   (United Kingdom)

^f BEAUMONT HOSPITAL   (Ireland)

Author keywords

Catechol O methyltransferase; D2 3 receptor binding; Dopamine; SPECT; Striatum

Indexed keywords

CATECHOL METHYLTRANSFERASE; DOPAMINE 2 RECEPTOR; DOPAMINE 3 RECEPTOR; METHIONINE; VALINE;

ADULT; ADULT DISEASE; ARTICLE; CHROMOSOME DELETION 22Q11; CLINICAL ARTICLE; CORPUS STRIATUM; DNA POLYMORPHISM; ENZYME ACTIVITY; FEMALE; GENETIC ANALYSIS; HEMIZYGOTE; HUMAN; MALE; PHOTON EMISSION TOMOGRAPHY; PRIORITY JOURNAL; RECEPTOR BINDING;

22Q11 DELETION SYNDROME; ADOLESCENT; ADULT; CATECHOL O-METHYLTRANSFERASE; CORPUS STRIATUM; FEMALE; GENOTYPE; HUMANS; MALE; METHIONINE; PROTEIN BINDING; RECEPTORS, DOPAMINE D2; RECEPTORS, DOPAMINE D3; TOMOGRAPHY, EMISSION-COMPUTED, SINGLE-PHOTON; VALINE; YOUNG ADULT;

EID: 79959946393     PISSN: 08874476     EISSN: 10982396     Source Type: Journal    
DOI: 10.1002/syn.20932     Document Type: Article

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