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	<title>Recash test site | Solis Mejer | Activity</title>
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				<title>Solis Mejer posted an update: e., CEP290, C5ORF, TCTN1, CC2D2A, RPGRP1L, TCTN3, AHI1, [&#133;]</title>
				<link>https://recash.wpsoul.net/activity/p/56839/</link>
				<pubDate>Thu, 12 Dec 2024 00:20:30 +0000</pubDate>

									<content:encoded><![CDATA[<p>e., CEP290, C5ORF, TCTN1, CC2D2A, RPGRP1L, TCTN3, AHI1, INPP5E, TCTN2, NPHP1, and TMEM237. For the first time, we identified a ciliopathy gene, CCDC28B, as a causal gene in Joubert syndrome in one family. CEP290 accounted for 37.8% cases of pure Joubert syndrome, Joubert syndrome with retinal and renal disease, and Meckel-Gruber syndrome. The&hellip;<span class="activity-read-more" id="activity-read-more-56839"><a href="https://recash.wpsoul.net/activity/p/56839/" rel="nofollow ugc">[Read more]</a></span></p>
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				<title>Solis Mejer became a registered member</title>
				<link>https://recash.wpsoul.net/activity/p/56707/</link>
				<pubDate>Thu, 12 Dec 2024 00:03:59 +0000</pubDate>

				
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