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Developmental excitatory-to-inhibitory GABA-polarity switch is disrupted in 22q11.2 deletion syndrome: a potential target for clinical therapeutics

Individuals with 22q11.2 microdeletion syndrome (22q11.2 DS) show cognitive and behavioral dysfunctions, developmental delays in childhood and risk of developing schizophrenia and autism. Despite extensive previous studies in adult animal models, a possible embryonic root of this syndrome has not be...

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Detalhes bibliográficos
Publicado no:Sci Rep
Main Authors: Amin, Hayder, Marinaro, Federica, De Pietri Tonelli, Davide, Berdondini, Luca
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2017
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5691208/
https://ncbi.nlm.nih.gov/pubmed/29146941
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-017-15793-9
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