Molecular Mechanisms of Rett Syndrome: Emphasizing the Roles of Monoamine, Immunity, and Mitochondrial Dysfunction

Molecular Mechanisms of Rett Syndrome: Emphasizing the Roles of Monoamine, Immunity, and Mitochondrial Dysfunction

Rett syndrome (RTT), which predominantly affects females, arises in most cases from mutations in the <i>Methyl-CpG-binding Protein-2</i> (<i>MECP2</i>) gene. When MeCP2 is impaired, it disrupts the regulation of numerous genes, causing the production of dysfunctional proteins...

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Bibliographic Details
Main Authors: Julia Lopes Gonçalez, Jenny Shen, Wei Li
Format: Article
Language:English
Published: MDPI AG 2024-12-01
Series:Cells
Subjects:
Rett syndrome
MeCP2
monoamine
immune cell
mitochondria
Online Access:https://www.mdpi.com/2073-4409/13/24/2077
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