No association of the norepinephrine transporter gene (SLC6A2) and cognitive and behavioural phenotypes of patients with autism spectrum disorder-Reference-Cited by-同舟云学术

No association of the norepinephrine transporter gene (SLC6A2) and cognitive and behavioural phenotypes of patients with autism spectrum disorder

Published:2014-01-01 Issue:6 Volume:264 Page:507-515
ISSN:0940-1334
Container-title:European Archives of Psychiatry and Clinical Neuroscience
language:en
Short-container-title:Eur Arch Psychiatry Clin Neurosci

Author:

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,Yoo Hee Jeong

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Biological Psychiatry,Psychiatry and Mental health,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00406-013-0480-6.pdf

Reference27 articles.

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3. Veenstra-Vanderweele J, Christian SL, Cook EH Jr (2004) Autism as a paradigmatic complex genetic disorder. Ann Rev Genomics Hum Genet 5:379–405. doi: 10.1146/annurev.genom.5.061903.180050

4. Kim SJ, Silva RM, Flores CG, Jacob S, Guter S, Valcante G, Zaytoun AM, Cook EH, Badner JA (2011) A quantitative association study of SLC25A12 and restricted repetitive behavior traits in autism spectrum disorders. Mol Autism 2(1):8. doi: 10.1186/2040-2392-2-8

5. Anderson GM (1987) Monoamines in autism: an update of neurochemical research on a pervasive developmental disorder. Med Biol 65(2–3):67–74

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