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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 V  Novakovic Ivana V  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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