eNauka - pregled
Pregled prema Autor Culav, Ljerka
Prikaz rezultata 1 do 1 od 1
| Godina | Naslov | Autor(i) | Tip rezultata | Mp-kat. |
|---|---|---|---|---|
| 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 |