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MeCP2 Deficiency in Neuroglia: New Progress in the Pathogenesis of Rett Syndrome

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Rett syndrome (RTT) is an X-linked neurodevelopmental disease predominantly caused by mutations of the methyl-CpG-binding protein 2 (MeCP2) gene. Generally. RTT has been attributed to neuron-centric dysfunction. However. https://www.adventuresportsusa.shop/product-category/kiteboarding-lesson/
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