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Altered Bone Status in Rett Syndrome

Rett syndrome (RTT) is a monogenic neurodevelopmental disorder primarily caused by mutations in X-linked MECP2 gene, encoding for methyl-CpG binding protein 2 (MeCP2), a multifaceted modulator of gene expression and chromatin organization. Based on the type of mutation, RTT patients exhibit a broad...

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Detalles Bibliográficos
Autores principales:	Pecorelli, Alessandra, Cordone, Valeria, Schiavone, Maria Lucia, Caffarelli, Carla, Cervellati, Carlo, Cerbone, Gaetana, Gonnelli, Stefano, Hayek, Joussef, Valacchi, Giuseppe
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2021
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8230033/ https://www.ncbi.nlm.nih.gov/pubmed/34205017 http://dx.doi.org/10.3390/life11060521

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