Biallelic RFC1 Expansions Are a Rare Cause of Early-Onset and Familial Parkinson's Disease

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Naziv:	Biallelic RFC1 Expansions Are a Rare Cause of Early-Onset and Familial Parkinson's Disease
Autori:	Kovanda, Anja; Šušmelj, Lara; Jaklič, Helena; Lukežič, Tadeja; Maver, Aleš; Petrović, Igor N. ; Dragašević-Mišković, Nataša T. ; Svetel, Marina V. ; Racki, Valentino; Vuletič, Vladimira; Novakovič, Ivana V. ; Peterlin, Borut;
Godina:	2025
Publikacija:	Clinical genetics
ISSN:	0009-9163 Clinical Genetics Pretraži identifikator
Izdavač:	Copenhagen, Munksgaard
Tip rezultata:	Informativni prilog
Kolacija:	vol. Online ahead of print
DOI:	10.1111/cge.70095
WoS-ID:	001607067300001
Scopus-ID:	2-s2.0-105020756382
PMID:	41177915
URI:	https://enauka.gov.rs/handle/123456789/1009212
URL:	https://onlinelibrary.wiley.com/doi/10.1111/cge.70095
Projekat:	Slovenian Research and Innovation Agency (ARIS) [P3-0326, J3-4517]
Izvor metapodataka:	(Preuzeto iz Nasi u WoS)
M-kategorija:	22M22 - Međunarodni časopis kategorije M22

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