Erratum: Genetic variants in COMT and neurocognitive impairment in families of patients with schizophrenia (Genes, Brain and Behavior (2009) 8, (228-237) DOI: 10.1111/j.1601-183X.2008.00467.x);Genetic variants in COMT and neurocognitive impairment in families of patients with schizophrenia

Genes, Brain and Behavior

Volumn 8, Issue 2, 2009, Pages 228-237

  Liao, S Y ^a,b   Lin, S H ^a,c   Liu, C M ^d   Hsieh, M H ^d   Hwang, T J ^d   Liu, S K ^d,e   Guo, S C ^f   Hwu, H G ^b,c,d   Chen, W J ^a,c,d,g  

^a Genetic Epidemiology Core Laboratory   (Taiwan)

^b School of Medicine

^c Institute of Occupational Medicine and Industrial Hygiene   (Taiwan)

^d NATIONAL TAIWAN UNIVERSITY HOSPITAL   (Taiwan)

^e FAR EASTERN MEMORIAL HOSPITAL   (Taiwan)

^f Ju Shan Mental Hospital   (Taiwan)

^g NATIONAL TAIWAN UNIVERSITY   (Taiwan)

Author keywords

COMT; Continuous performance test; Family based association study; Gene; Quantitative trait; Schizophrenia; Wisconsin Card Sorting Test

Indexed keywords

CATECHOL METHYLTRANSFERASE;

ADULT; ARTICLE; COGNITIVE DEFECT; CONTINUOUS PERFORMANCE TEST; FAMILY STUDY; FEMALE; HUMAN; HUMAN TISSUE; MAJOR CLINICAL STUDY; MALE; MENTAL PERFORMANCE; MENTAL TEST; PRIORITY JOURNAL; RESPONSE TIME; SCHIZOPHRENIA; SINGLE NUCLEOTIDE POLYMORPHISM; WISCONSIN CARD SORTING TEST;

EID: 61449117923     PISSN: 16011848     EISSN: 1601183X     Source Type: Journal    
DOI: 10.1111/j.1601-183X.2009.00541.x     Document Type: Erratum

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