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Rett syndrome (RTT) is a neurodevelopmental disability characterized by mutations in the X‐linked methyl‐CpG‐binding protein 2 located at the Xq28 region. The severity is modified in part by X chromosomal inactivation resulting in wide clinical variability. We hypothesized that the ability to perform the activities of daily living (ADL) is correlated with the density of vesicular acetylcholine transporters...
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