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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Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Life (Basel)
Asıl Yazarlar: Pecorelli, Alessandra, Cordone, Valeria, Schiavone, Maria Lucia, Caffarelli, Carla, Cervellati, Carlo, Cerbone, Gaetana, Gonnelli, Stefano, Hayek, Joussef, Valacchi, Giuseppe
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: MDPI 2021
Konular:
Review
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC8230033/
https://ncbi.nlm.nih.gov/pubmed/34205017
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/life11060521
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