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Naslov Biallelic RFC1 expansions as a rare cause of familial and early onset Parkinson's disease in the Slavic population (Meeting Abstract)
Autori Kovanda Anja  Susmelj Lara  Lukezic Tadeja  Maver Ales  Racki Valentino  Vuletic Vladimira  Svetel Marina  Novakovic Ivana  Peterlin Borut 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2025), vol. 33 br. , Suppl. 1, str. 797-798
Ispravka ISI/Web of Science   Elečas   Rang časopisa  
Naslov Biallelic RFC1 Expansions Are a Rare Cause of Early-Onset and Familial Parkinson's Disease (Editorial Material; Early Access)
Autori Kovanda Anja  Susmelj Lara  Jaklic Helena  Lukezic Tadeja  Maver Ales  Petrovic Igor N  Dragasevic-Miskovic Natasa T  Svetel Marina V  Racki Valentino  Vuletic Vladimira  Novakovic Ivana V  Peterlin Borut 
Info CLINICAL GENETICS, (2025), vol. br. , str. -
Projekat Slovenian Research and Innovation Agency (ARIS) [P3-0326, J3-4517]
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