The CC2D2B is a novel genetic modifier of the clinical phenotype in patients with hereditary angioedema due to C1 inhibitor deficiency
Journal article published in 2024 by
Nina Rupar,
Julij Šelb,
Mitja Košnik,
Mihaela Zidarn,
Slađana Andrejević,
Ljerka Čulav,
Vesna Grivčeva‐Panovska 
,
Peter Korošec,
Matija Rijavec
,
Peter Korošec,
Matija Rijavec
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