HDAC inhibitor ameliorates behavioral deficits in Mecp2 308/y mouse model of Rett syndrome
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DOI: 10.1016/j.brainres.2021.147670
Abstract: Rett syndrome (RTT) is a rare X-linked neurodevelopmental disorder. More than 95% of classic RETT syndrome cases result from pathogenic variants in the methyl-CpG binding protein 2 (MECP2) gene. Nevertheless, it has been established that… read more here.
Keywords: inhibitor ameliorates; rett syndrome; mecp2 308; mecp2 deficient ... See more keywords