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<metadata xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/"><dc:title>In vivo delivery strategies for therapeutic CRISPR genome editing</dc:title><dc:creator>Martin,	Leonardo	(Avtor)
	</dc:creator><dc:creator>Bohinc,	Jure	(Avtor)
	</dc:creator><dc:creator>Recchia,	Alessandra	(Avtor)
	</dc:creator><dc:creator>Gritti,	Stefano	(Avtor)
	</dc:creator><dc:creator>Santilli,	Giorgia	(Avtor)
	</dc:creator><dc:creator>Skrbinek,	Mojca	(Avtor)
	</dc:creator><dc:creator>Mlakar,	Tjaša	(Avtor)
	</dc:creator><dc:creator>Lapanja,	Tjaša	(Avtor)
	</dc:creator><dc:date>2026</dc:date><dc:date>2026-08-04 12:51:48</dc:date><dc:type>Neznano</dc:type><dc:identifier>31509</dc:identifier><dc:identifier>UDK: 577</dc:identifier><dc:identifier>ISSN pri članku: 1449-2288</dc:identifier><dc:identifier>DOI: 10.7150/ijbs.133162</dc:identifier><dc:identifier>COBISS_ID: 286080771</dc:identifier><dc:language>sl</dc:language><dc:rights>© The author(s). This is an open access article distributed under the terms of the Creative Commons Attribution License</dc:rights></metadata>
