Additional file 5 of Regulation of human microglial gene expression and function via RNAase-H active antisense oligonucleotides in vivo in Alzheimer’s disease
MECP2 duplication syndrome, a childhood neurological disorder characterized by autism, intellectual disability, motor dysfunction, anxiety and epilepsy, is caused by a duplication on chromosome Xq28 s
References listed indicate studies that have confirmed the effectiveness of these MO sequences. Note that no p58b or p16 sequences have ever been tested with Vivo-Morpholinos.Vivo-Morpholino sequences