<i>MECP2</i>-Related Disorders in Males
Methyl CpG binding protein 2 (<i>MECP2</i>) is located at Xq28 and is a multifunctional gene with ubiquitous expression. Loss-of-function mutations in <i>MECP2</i> are associated with Rett syndrome (RTT), which is a well-characterized disorder that affects mainly females. In...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2021-09-01
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| Series: | International Journal of Molecular Sciences |
| Subjects: | |
| Online Access: | https://www.mdpi.com/1422-0067/22/17/9610 |