Polyhydramnios megalencephaly and symptomatic epilepsy syndrome (PMSE) is a uncommon individual autosomal-recessive disorder seen as a abnormal human brain development cognitive impairment and intractable epilepsy. this further we modeled PMSE in mouse neural progenitor cells (mNPCs) in vitro and in developing mouse cortex in vivo by knocking down STRADĪ± appearance. STRADĪ±-lacking mNPCs were showed and… Continue reading Polyhydramnios megalencephaly and symptomatic epilepsy syndrome (PMSE) is a uncommon individual