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Autori: Rupar Nina

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Naslov The CC2D2B is a novel genetic modifier of the clinical phenotype in patients with hereditary angioedema due to C1 inhibitor deficiency (Article)
Autori Rupar Nina  Selb Julij  Kosnik Mitja  Zidarn Mihaela  Andrejevic Sladjana B  Culav Ljerka  Grivceva-Panovska Vesna  Korosec Peter  Rijavec Matija 
Info GENE, (2024), vol. 919 br. , str. -
Projekat Slovenian Research and Inno-vation Agency [P3-0360, J3-2532]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
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