Genes regulated by SATB2 during neurodevelopment contribute to schizophrenia and educational attainment

SATB2 is associated with schizophrenia and is an important transcription factor regulating neocortical organization and circuitry. Rare mutations in SATB2 cause a syndrome that includes developmental delay, and mouse studies identify an important role for SATB2 in learning and memory. Interacting pa...

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Detalles Bibliográficos
Autores principales: Whitton, Laura, Apostolova, Galina, Rieder, Dietmar, Dechant, Georg, Rea, Stephen, Donohoe, Gary, Morris, Derek W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097700/
https://www.ncbi.nlm.nih.gov/pubmed/30040823
http://dx.doi.org/10.1371/journal.pgen.1007515

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097700/
https://www.ncbi.nlm.nih.gov/pubmed/30040823
http://dx.doi.org/10.1371/journal.pgen.1007515

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