Functional analysis of MeCP2 in astrocyte
收藏NIAID Data Ecosystem2026-03-13 收录
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资源简介：
Rett syndrome (RTT) is a severe neurodevelopmental disorder affecting almost exclusively females. RTT is caused by sporadic mutations in the X- linked transcriptional regulator methyl-CpG binding protein 2 (MECP2) gene. Recent studies show that MeCP2 is expressed and functions in not only neuron but also glial cells. Our goal is to understand the role of MeCP2 in astrocyte.
创建时间：
2025-09-30
