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...
Main Authors: | , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2018-07-01
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Series: | PLoS Genetics |
Online Access: | http://europepmc.org/articles/PMC6097700?pdf=render |