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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 <i>MECP2</i> 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...

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Sparad:
Huvudupphov: Alessandra Pecorelli, Valeria Cordone, Maria Lucia Schiavone, Carla Caffarelli, Carlo Cervellati, Gaetana Cerbone, Stefano Gonnelli, Joussef Hayek, Giuseppe Valacchi
Materialtyp: Artigo
Språk:Inglês
Utgiven: MDPI AG 2021-06-01
Serie:Life
Ämnen:
MeCP2
bone mineral density
bone metabolism
osteoblast
WNT pathway
Länkar:https://www.mdpi.com/2075-1729/11/6/521
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