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<oembed><version>1.0</version><provider_name>Achucarro Basque Center for Neuroscience</provider_name><provider_url>https://www.achucarro.org/es/</provider_url><title>Angelman Syndrome causing UBE3A ligase displays predominantly synaptic ubiquitination activity in the mouse brain - Achucarro Basque Center for Neuroscience</title><type>rich</type><width>600</width><height>338</height><html>&lt;blockquote class="wp-embedded-content" data-secret="wIyZr6p0zh"&gt;&lt;a href="https://www.achucarro.org/es/seminario/2023-05-ugo-mayor/"&gt;Angelman Syndrome causing UBE3A ligase displays predominantly synaptic ubiquitination activity in the mouse brain&lt;/a&gt;&lt;/blockquote&gt;&lt;iframe sandbox="allow-scripts" security="restricted" src="https://www.achucarro.org/es/seminario/2023-05-ugo-mayor/embed/#?secret=wIyZr6p0zh" width="600" height="338" title="&#xAB;Angelman Syndrome causing UBE3A ligase displays predominantly synaptic ubiquitination activity in the mouse brain&#xBB; &#x2014; Achucarro Basque Center for Neuroscience" data-secret="wIyZr6p0zh" frameborder="0" marginwidth="0" marginheight="0" scrolling="no" class="wp-embedded-content"&gt;&lt;/iframe&gt;&lt;script&gt;
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</html><description>Angelman Syndrome (AS) is a neurodevelopmental disorder with complex symptomatology caused by the loss of maternal allele expression of one single gene in the brain, the ubiquitin E3 ligase UBE3A. The underlying genetic basis of AS, and the phenotypes observed in both humans and in animal models of AS, have previously been extensively described. However, [&hellip;]</description></oembed>
