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Browsing by Author Selb, Julij
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| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2024 | The CC2D2B is a novel genetic modifier of the clinical phenotype in patients with hereditary angioedema due to C1 inhibitor deficiency | Rupar, Nina; Selb, Julij; Kosnik, Mitja; Zidarn, Mihaela; Andrejevic, Sladjana B; Culav, Ljerka; Grivceva-Panovska, Vesna; Korosec, Peter; Rijavec, Matija | Article | 21M21 |