A Plasma Proteomic Approach in Rett Syndrome: Classical versus Preserved Speech Variant
Rett syndrome (RTT) is a progressive neurodevelopmental disorder mainly caused by mutations in the gene encoding the methyl-CpG-binding protein 2 (MeCP2). Although over 200 mutations types have been identified so far, nine of which the most frequent ones. A wide phenotypical heterogeneity is a well-...
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Main Authors: | , , , , , , , , , , , , |
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Format: | Book |
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Hindawi Limited,
2013-01-01T00:00:00Z.
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A1234.567 |
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