Mitochondrial Proteome Changes in Rett Syndrome
Rett syndrome (RTT) is a genetic neurodevelopmental disorder with mutations in the X-chromosomal <i>MECP2</i> (methyl-CpG-binding protein 2) gene. Most patients are young girls. For 7–18 months after birth, they hardly present any symptoms; later they develop mental problems, a lack of c...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2023-07-01
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| Series: | Biology |
| Subjects: | |
| Online Access: | https://www.mdpi.com/2079-7737/12/7/956 |