Electroencephalographic spectral power as a marker of cortical function and disease severity in girls with Rett syndrome
Abstract Background Rett syndrome is a neurodevelopmental disorder caused by a mutation in the X-linked MECP2 gene. Individuals with Rett syndrome typically develop normally until around 18 months of age before undergoing a developmental regression, and the disorder can lead to cognitive, motor, sen...
में बचाया:
| मुख्य लेखकों: | , , , , , |
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| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
BMC
2019-07-01
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| श्रृंखला: | Journal of Neurodevelopmental Disorders |
| विषय: | |
| ऑनलाइन पहुंच: | http://link.springer.com/article/10.1186/s11689-019-9275-z |
| टैग: |
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