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eNauka >  Rezultati >  Biallelic RFC1 Expansions Are a Rare Cause of Early-Onset and Familial Parkinson's Disease
Title: Biallelic RFC1 Expansions Are a Rare Cause of Early-Onset and Familial Parkinson's Disease
Authors: 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;
Issue Date: 2025
Publication: Clinical genetics
ISSN: 0009-9163 Clinical Genetics Search Idenfier
Publisher: Copenhagen, Munksgaard
Type: Contribution to periodical
Collation: 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
Project: Slovenian Research and Innovation Agency (ARIS) [P3-0326, J3-4517]
Metadata source: (Preuzeto iz Nasi u WoS)
M-category: 
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