Analysis of Astroglial Secretomic Profile in the Mecp2-Deficient Male Mouse Model of Rett Syndrome
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DOI: 10.3390/ijms22094316
Abstract: Mutations in the X-linked MECP2 gene are responsible for Rett syndrome (RTT), a severe neurological disorder. MECP2 is a transcriptional modulator that finely regulates the expression of many genes, specifically in the central nervous system.… read more here.
Keywords: analysis astroglial; rett syndrome; mecp2; mecp2 deficient ... See more keywords