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Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome

The 22q11 deletion (or DiGeorge) syndrome (22q11DS), the result of a 1.5- to 3-megabase hemizygous deletion on human chromosome 22, results in dramatically increased susceptibility for “diseases of cortical connectivity” thought to arise during development, including schizophrenia and autism. We sho...

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Detalhes bibliográficos
Main Authors: Meechan, Daniel W., Tucker, Eric S., Maynard, Thomas M., LaMantia, Anthony-Samuel
Formato: Artigo
Idioma:Inglês
Publicado em: National Academy of Sciences 2009
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2752572/
https://ncbi.nlm.nih.gov/pubmed/19805316
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0905696106
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