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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 Web of Science   Članak   Elečas   Rang časopisa  
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Naslov Hereditary angioedema due to C1-inhibitor deficiency in south-eastern Europe: SERPING1 mutations and genetic factors modifying the clinical phenotype (Meeting Abstract)
Autori Rijavec Matija Kosnik Mitja Zidarn M Andrejevic Sladjana B Karadza-Lapic Ljerka Cikojevic D Grivceva-Panovska Vesna Korosec Peter 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 2, str. 1360-1361
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science  
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Naslov The functional promoter F12-46C/T variant predicts the asymptomatic phenotype of C1-INH-HAE (Letter)
Autori Rijavec Matija Kosnik Mitja Andrejevic Sladjana B Karadza-Lapic Ljerka Grivceva-Panovska Vesna Korosec Peter 
Info CLINICAL AND EXPERIMENTAL ALLERGY, (2019), vol. 49 br. 11, str. 1520-1522
Projekat Javna Agencija za Raziskovalno Dejavnost RS [P3-0360]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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