Huntingtin phosphorylation governs BDNF homeostasis and improves the phenotype of Mecp2 knockout mice
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DOI: 10.15252/emmm.201910889
Abstract: Mutations in the X‐linked MECP2 gene are responsible for Rett syndrome (RTT), a severe neurological disorder for which there is no treatment. Several studies have linked the loss of MeCP2 function to alterations of brain‐derived… read more here.
Keywords: phenotype mecp2; mecp2 knockout; mecp2; mice ... See more keywords