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The CC2D2B is a novel genetic modifier of the clinical phenotype in patients with hereditary angioedema due to C1 inhibitor deficiency
| Title: | The CC2D2B is a novel genetic modifier of the clinical phenotype in patients with hereditary angioedema due to C1 inhibitor deficiency | Authors: | Rupar, Nina; Selb, Julij; Kosnik, Mitja; Zidarn, Mihaela; Andrejevic, Sladjana B; Culav, Ljerka; Grivceva-Panovska, Vesna; Korosec, Peter; Rijavec, Matija | Issue Date: | 2024 | Publication: | GENE | ISSN: | 0378-1119 Gene Search Idenfier |
Type: | Article | Collation: | vol. 919 str. 148496-148496 | DOI: | 10.1016/j.gene.2024.148496 | WoS-ID: | 001238525200001 | Scopus-ID: | 2-s2.0-85191870984 | URI: | https://enauka.gov.rs/handle/123456789/937692 | Project: | Slovenian Research and Inno-vation Agency [P3-0360, J3-2532] | Metadata source: | (Preuzeto iz Nasi u WoS) | M-category: | 21M21 |
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