MECP2 mutations affect ciliogenesis: a novel perspective for Rett syndrome and related disorders
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DOI: 10.15252/emmm.201910270
Abstract: Mutations in MECP2 cause several neurological disorders of which Rett syndrome (RTT) represents the best‐defined condition. Although mainly working as a transcriptional repressor, MeCP2 is a multifunctional protein revealing several activities, the involvement of which… read more here.
Keywords: ciliogenesis; affect ciliogenesis; rett syndrome; mutations affect ... See more keywords