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    <title>Mitochondrial Genetic Disease on Notaspampeanas</title>
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      <title>CONICET-UBA: Achievement on key progress against a serious genetic disease</title>
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      <pubDate>Mon, 02 Mar 2026 00:18:24 -0300</pubDate>
      
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  Specialists from &lt;strong&gt;CONICET&lt;/strong&gt; and &lt;strong&gt;UBA&lt;/strong&gt; managed, in vitro studies, to stabilize defective proteins associated with &lt;a href=&#34;https://en.wikipedia.org/wiki/Friedreich%27s_ataxia&#34; target=&#34;_blank&#34;&gt;Friedreich&amp;rsquo;s ataxia&lt;/a&gt;, a degenerative disorder that still has no cure. The work, which is part of a line of research that has an international grant, opens up new therapeutic possibilities.
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&lt;strong&gt;Interaction between frataxin (key protein in Friedreich&amp;rsquo;s ataxia) and a nanoantibody (in red and blue) Image credit: María Florencia Pignataro, Juan A. Hermoso, Lorena Itatí Ibáñez, Javier Santos et al..&lt;/strong&gt;&lt;/p&gt;</description>
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