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eNauka >  Results >  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: 
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