Developmental disruption to the cortical transcriptome and synaptosome in a model of SETD1A loss-of-function

Overview of attention for article published in Human Molecular Genetics, May 2022

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Interesting SCZ mouse model connecting rare LOF of histone modifier SETD1A w/ mitoch dysfcn and synaptic proteome changes. https://t.co/Z8GNwuVpxC

RT @NE_Clifton: Using multi-omics, we observed prenatal and postnatal disruption to (nuclear-encoded) mitochondrial pathways in a model of…

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