{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,27]],"date-time":"2026-09-27T14:17:53Z","timestamp":1790518673003,"version":"4.1.0"},"reference-count":70,"publisher":"S. Karger AG","issue":"3-5","license":[{"start":{"date-parts":[[2011,1,1]],"date-time":"2011-01-01T00:00:00Z","timestamp":1293840000000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/www.karger.com\/Services\/SiteLicenses"},{"start":{"date-parts":[[2011,1,1]],"date-time":"2011-01-01T00:00:00Z","timestamp":1293840000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.karger.com\/Services\/SiteLicenses"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Mol Syndromol"],"published-print":{"date-parts":[[2011]]},"abstract":"<jats:p>Rett syndrome is one of the most common causes of complex disability in girls. It is characterized by early neurological regression that severely affects motor, cognitive and communication skills, by autonomic dysfunction and often a seizure disorder. It is a monogenic X-linked dominant neurodevelopmental disorder related to mutation in &lt;i&gt;MECP2&lt;\/i&gt;, which encodes the methyl-CpG-binding protein MeCP2. There are several mouse models either based on conditional knocking out of the &lt;i&gt;Mecp2&lt;\/i&gt; gene or on a truncating mutation. We discuss the clinical aspects with special emphasis on the behavioral phenotype and we review current perspectives in clinical management alongside with perspectives in altering gene expression.<\/jats:p>","DOI":"10.1159\/000337637","type":"journal-article","created":{"date-parts":[[2012,4,18]],"date-time":"2012-04-18T03:46:27Z","timestamp":1334720787000},"page":"113-127","source":"Crossref","is-referenced-by-count":90,"title":["Rett 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