Search Results - "Miramondi, Federica"

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    Identification of Region-Specific Cytoskeletal and Molecular Alterations in Astrocytes of Mecp2 Deficient Animals by Albizzati, Elena, Florio, Elena, Miramondi, Federica, Sormonta, Irene, Landsberger, Nicoletta, Frasca, Angelisa

    Published in Frontiers in neuroscience (15-02-2022)
    “…Rett syndrome (RTT) is a neurodevelopmental disorder that represents the most common genetic cause of severe intellectual disability in females. Most patients…”
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