Brain protein changes in Mecp2 mouse mutant models: Effects on disease progression of Mecp2 brain specific gene reactivation.
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DOI: 10.1016/j.jprot.2019.103537
Abstract: Rett syndrome (RTT) is a leading cause of severe intellectual disability in females, caused by de novo loss-of function mutations in the X-linked methyl-CpG binding protein 2 (MECP2). To better investigate RTT disease progression/pathogenesis animal… read more here.
Keywords: protein; mecp2 mouse; mecp2; disease progression ... See more keywords