Subclinical Inflammatory Status in Rett Syndrome
Inflammation has been advocated as a possible common central mechanism for developmental cognitive impairment. Rett syndrome (RTT) is a devastating neurodevelopmental disorder, mainly caused by de novo loss-of-function mutations in the gene encoding MeCP2. Here, we investigated plasma acute phase re...
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Main Authors: | , , , , , , , , , , , |
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Format: | Book |
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Hindawi Limited,
2014-01-01T00:00:00Z.
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Online Access: | Connect to this object online. |
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