Genomic and epigenetic evidence for oxytocin receptor deficiency in autism

BACKGROUND: Autism comprises a spectrum of behavioral and cognitive disturbances of childhood development and is known to be highly heritable. Although numerous approaches have been used to identify genes implicated in the development of autism, less than 10% of autism cases have been attributed to...

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Detalles Bibliográficos
Autores principales: Gregory, Simon G, Connelly, Jessica J, Towers, Aaron J, Johnson, Jessica, Biscocho, Dhani, Markunas, Christina A, Lintas, Carla, Abramson, Ruth K, Wright, Harry H, Ellis, Peter, Langford, Cordelia F, Worley, Gordon, Delong, G Robert, Murphy, Susan K, Cuccaro, Michael L, Persico, Antonello, Pericak-Vance, Margaret A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2774338/
https://www.ncbi.nlm.nih.gov/pubmed/19845972
http://dx.doi.org/10.1186/1741-7015-7-62

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2774338/
https://www.ncbi.nlm.nih.gov/pubmed/19845972
http://dx.doi.org/10.1186/1741-7015-7-62

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