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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| Autors principals: | , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
MDPI AG
2021-06-01
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| Col·lecció: | Life |
| Matèries: | |
| Accés en línia: | https://www.mdpi.com/2075-1729/11/6/521 |
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