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		<title>MFSD2A-associated primary microcephaly &#8211; Expanding the clinical and mutational spectrum of this ultra-rare disease</title>
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		<dc:creator><![CDATA[Susann Meyer]]></dc:creator>
		<pubDate>Fri, 13 Aug 2021 07:57:35 +0000</pubDate>
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		<category><![CDATA[Wollnik, Bernd]]></category>
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					<description><![CDATA[Khuller K, Yigit G, Grijalva CM, Altmüller J, Thiele H, Nürnberg P, Elcioglu NH, Yeter B, Hehr U, Stein A, Della Marina A, Köninger A, Depienne C, Kaiser FJ, Wollnik B, Kuechler A]]></description>
		
		
		
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