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	Comments on: Genome editing of liver organoids for treatment of alpha-1 antitrypsin deficiency.	</title>
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		By: Giles Hider		</title>
		<link>https://childliverdisease.org/genome-editing-of-liver-organoids-for-treatment-of-alpha-1-antitrypsin-deficiency/#comment-8827</link>

		<dc:creator><![CDATA[Giles Hider]]></dc:creator>
		<pubDate>Sun, 24 Nov 2024 09:11:11 +0000</pubDate>
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					<description><![CDATA[As someone who has A1ATD, I wish Professor Deborah Gill all the best with her research and I hope one day it will provide a cure… for me it will be too late and now a recipient of a Lover transplant… but I have supported research throughout my life to research and my hope is that future generations will be cured without needing a transplant… all the best <img src="https://s.w.org/images/core/emoji/17.0.2/72x72/2665.png" alt="♥" class="wp-smiley" style="height: 1em; max-height: 1em;" /><img src="https://s.w.org/images/core/emoji/17.0.2/72x72/1f44f.png" alt="👏" class="wp-smiley" style="height: 1em; max-height: 1em;" />]]></description>
			<content:encoded><![CDATA[<p>As someone who has A1ATD, I wish Professor Deborah Gill all the best with her research and I hope one day it will provide a cure… for me it will be too late and now a recipient of a Lover transplant… but I have supported research throughout my life to research and my hope is that future generations will be cured without needing a transplant… all the best ♥️👏</p>
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