A genetic variant that disrupts MET transcription is associated with autism

There is strong evidence for a genetic predisposition to autism and an intense interest in discovering heritable risk factors that disrupt gene function. Based on neurobiological findings and location within a chromosome 7q31 autism candidate gene region, we analyzed the gene encoding the pleiotropi...

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Detalhes bibliográficos
Main Authors: Campbell, Daniel B., Sutcliffe, James S., Ebert, Philip J., Militerni, Roberto, Bravaccio, Carmela, Trillo, Simona, Elia, Maurizio, Schneider, Cindy, Melmed, Raun, Sacco, Roberto, Persico, Antonio M., Levitt, Pat
Formato: Artigo
Idioma:Inglês
Publicado em: National Academy of Sciences 2006
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1838551/
https://ncbi.nlm.nih.gov/pubmed/17053076
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0605296103
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https://ncbi.nlm.nih.gov/pmc/articles/PMC1838551/
https://ncbi.nlm.nih.gov/pubmed/17053076
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0605296103