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The CC2D2B is a novel genetic modifier of the clinical phen..:
Rupar, Nina
;
Šelb, Julij
;
Košnik, Mitja
...
Gene. 919 (2024) - p. 148496 , 2024
Link:
https://doi.org/10.1016/j.gene.2024.148496
RT Journal T1
The CC2D2B is a novel genetic modifier of the clinical phenotype in patients with hereditary angioedema due to C1 inhibitor deficiency
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.gene.2024.148496&Exemplar=1&LAN=DE A1 Rupar, Nina A1 Šelb, Julij A1 Košnik, Mitja A1 Zidarn, Mihaela A1 Andrejević, Slađana A1 Čulav, Ljerka A1 Grivčeva‐Panovska, Vesna A1 Korošec, Peter A1 Rijavec, Matija PB Elsevier BV YR 2024 SN 0378-1119 JF Gene VO 919 SP 148496 LK http://dx.doi.org/https://doi.org/10.1016/j.gene.2024.148496 DO https://doi.org/10.1016/j.gene.2024.148496 SF ELIB - SuUB Bremen
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