Changes in the Cerebrospinal Fluid and Plasma Lipidome in Patients with Rett Syndrome
Rett syndrome (RTT) is defined as a rare disease caused by mutations of the methyl‐CpG binding protein 2 (MECP2). It is one of the most common causes of genetic mental retardation in girls, characterized by normal early psychomotor development, followed by severe neurologic regression. Hitherto, RTT...
| Main Authors: | , , , , , , , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
MDPI
2022
|
| Subjects: | |
| Online Access: | View Fulltext in Publisher |