No association of the norepinephrine transporter gene (SLC6A2) and cognitive and behavioural phenotypes of patients with autism spectrum disorder - Park, Subin; Park, Jong-Eun; Cho, Soo-Churl; Kim, Bung-Nyun; Shin, Min-Sup; Kim, Jae-Won; Cho, In Hee; Kim, Soon Ae; Park, Mira; Park, Tae-Won; Son, Jung-Woo; Chung, Un-Sun; et al. (European archives of psychiatry and clinical neuroscience, 2014)
Keywords: Adolescent; Autism; Behavioral Symptoms - etiology; Behavioral Symptoms - genetics; Child; Child Development Disorders, Pervasive - complications; Child Development Disorders, Pervasive - genetics; Child, Preschool; Cognition Disorders - etiology; Cognition Disorders - genetics; Female; Genetic Association Studies; Humans; Infant; Intelligence; Male; Medicine; Medicine & Public Health; Mutation - genetics; Neuropsychological Tests; Neurosciences; Norepinephrine Plasma Membrane Transport Proteins - genetics; Original Paper; Phenotype; Psychiatric Status Rating Scales; Psychiatry; Severity of Illness Index; Young Adult; Haplotype; Phenotype; Autism spectrum disorder