Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorder

Previous studies have provided conflicting evidence regarding the association of the serotonin transporter (5-HTT) gene with autism. Two polymorphisms have been identified in the human 5-HTT gene, a VNTR in intron 21 and a functional deletion/insertion in the promoter region (5-HTTLPR) with short an...

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Detalhes bibliográficos
Main Authors: Betancur, Catalina, Corbex, Marylis, Spielewoy, Cécile, Philippe, Anne, Laplanche, Jean-Louis, Launay, Jean-Marie, Gillberg, Christopher, Mouren-Simeoni, Marie-Christine, Hamon, Michel, Giros, Bruno, Nosten-Bertrand, Marika, Leboyer, Marion
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group Specialist Journals 2002
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1896269/
https://ncbi.nlm.nih.gov/pubmed/11803447
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/sj.mp.4001923
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