Article
Aberrant gliogenesis and excitation in MEF2C autism patient hiPSC-neurons and cerebral organoids
2020-11-19
Abstract excerpt
MEF2C has been shown to be a critical transcription factor for neurodevelopment, whose loss-of-function mutation in humans results in MEF2C haploinsufficiency syndrome (MHS), a severe form of autism spectrum disorder (ASD)/intellectual disability (ID). Here, we use patient hiPSC-derived cerebrocortical neurons and cerebral organoids to characterize MHS deficits. Unexpectedly, we found an aberrant micro-RNA-mediate...
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Identifiers and source
- Literature Corpus work
- 59d39454-431b-5d08-a1ee-c178675bc75a
- DOI
- 10.1101/2020.11.19.387639
