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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 [Elektronski vir]Rupar, Nina, 1992- ...Source: Gene [Elektronski vir]. - ISSN 1879-0038 (Vol. 919, [article no.] 148496, 2024, str. 1-11)Type of material - e-article ; adult, seriousPublish date - 2024Language - englishCOBISS.SI-ID - 194844163
Author
Rupar, Nina, 1992- |
Šelb, Julij |
Košnik, Mitja |
Zidarn, Mihaela |
Andrejević, Slađana |
Čulav, Ljerka |
Grivčeva-Panovska, Vesna |
Korošec, Peter, 1970- |
Rijavec, Matija
Topics
hereditarni angioedem |
pomanjkanje zaviralca C1 |
geni modifikatorji |
klinični fenotip |
povezave genotip-fenotip |
genetska varianta |
SERPING1 |
CC2D2B |
hereditary angioedema |
C1 inhibitor deficiency |
genetic modifiers |
clinical phenotype |
genotype-phenotype correlation |
genetic variant |
SERPING1 |
CC2D2B
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Database name | Field | Year |
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Links to authors' personal bibliographies | Links to information on researchers in the SICRIS system |
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Rupar, Nina, 1992- | |
Šelb, Julij | 36479 |
Košnik, Mitja | 10921 |
Zidarn, Mihaela | 25317 |
Andrejević, Slađana | |
Čulav, Ljerka | |
Grivčeva-Panovska, Vesna | |
Korošec, Peter, 1970- | 22807 |
Rijavec, Matija | 29300 |
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