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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>Biallelic RFC1 expansions are a rare cause of early-onset and familial Parkinson's disease</dc:title><dc:creator>Kovanda,	Anja	(Avtor)
	</dc:creator><dc:creator>Šušmelj,	Lara	(Avtor)
	</dc:creator><dc:creator>Jaklič,	Helena	(Avtor)
	</dc:creator><dc:creator>Lukežič,	Tadeja	(Avtor)
	</dc:creator><dc:creator>Maver,	Aleš	(Avtor)
	</dc:creator><dc:creator>Petrović,	Igor N.	(Avtor)
	</dc:creator><dc:creator>Peterlin,	Borut	(Avtor)
	</dc:creator><dc:subject>CANVAS</dc:subject><dc:subject>neurodegenerative disease</dc:subject><dc:subject>vestibular areflexia syndrome</dc:subject><dc:subject>CANVAS</dc:subject><dc:subject>RFC1</dc:subject><dc:subject>PCR</dc:subject><dc:date>2026</dc:date><dc:date>2026-03-18 14:24:20</dc:date><dc:type>Neznano</dc:type><dc:identifier>28413</dc:identifier><dc:identifier>UDK: 61:575</dc:identifier><dc:identifier>ISSN pri članku: 1399-0004</dc:identifier><dc:identifier>DOI: 10.1111/cge.70095</dc:identifier><dc:identifier>COBISS_ID: 256091651</dc:identifier><dc:language>sl</dc:language></metadata>
