Art

J-GLOBAL ID：201302215063610675   Reference number：13A0150615

SHANK3 as an autism spectrum disorder-associated gene

自閉症スペクトラム障害に関連する遺伝子SHANK3

Author (2)： UCHINO Shigeo (Dep. of Neurochemistry, National Inst. of Neuroscience, National Center of Neurology and Psychiatry, Kodaira, Tokyo ...) ,  WAGA Chikako (Dep. of Neurochemistry, National Inst. of Neuroscience, National Center of Neurology and Psychiatry, Kodaira, Tokyo ...)
Material： Brain & Development  (Brain & Dev)
Volume： 35  Issue： 2  Page： 106-110  Publication year： Feb. 2013 
JST Material Number： W0814A  ISSN： 0387-7604  Document type： Article
Article type： 文献レビュー  Country of issue： Netherlands (NLD)  Language： ENGLISH (EN)

Thesaurus term： *autism ,...
Semi thesaurus term： Phelan-McDermid syndrome ,...

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JST classification (2)： Mental disorders  (GR03000A) ,  Basic psychiatry  (GR01020I)

Reference (28)：

• Mefford HC, Batshaw ML, Hoffman EP. Genomics, intellectual disability, and autism. N Engl J Med 2012;366:733-43.
• Phelan MC, Rogers RC, Saul RA, Stapleton GA, Sweet K, McDermid H, et al. 22q13 deletion syndrome. Am J Med Genet 2001;101:91-9.
• Philippe A, Boddaert N, Vaivre-Douret L, Robel L, Danon-Boileau L, Malan V, et al. Neurobehavioral profile and brain imaging study of the 22q13.3 deletion syndrome in childhood. Pediatrics 2008;122:e376-82.
• Bonaglia MC, Giorda R, Borgatti R, Felisari G, Gagliardi C, Selicorni A, et al. Disruption of the ProSAP2 gene in a t(12;22)(q24.1;q13.3) is associated with the 22q13.3 deletion syndrome. Am J Hum Genet 2001;69:261-8.
• Bonaglia MC, Giorda R, Mani E, Aceti G, Anderlid B-M, Baroncini A, et al. Identification of a recurrent breakpoint within the SHANK3 gene in the 22q13.3 deletion syndrome. J Med Genet 2006;43:822-8.

Terms in the title (2)： 自閉症スペクトラム障害 ,  遺伝子