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Altered thalamocortical development in the SAP102 knockout model of intellectual disability

Genetic mutations known to cause intellectual disabilities (IDs) are concentrated in specific sets of genes including both those encoding synaptic proteins and those expressed during early development. We have characterized the effect of genetic deletion of Dlg3, an ID-related gene encoding the syna...

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Detalhes bibliográficos
Publicado no:Hum Mol Genet
Main Authors: Crocker-Buque, Alex, Currie, Stephen P., Luz, Liliana L., Grant, Seth G., Duffy, Kevin R., Kind, Peter C., Daw, Michael I.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2016
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5291236/
https://ncbi.nlm.nih.gov/pubmed/27466188
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddw244
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