Common variable immunodeficiency in two kindreds with heterogeneous phenotypes caused by novel heterozygous NFKB1 mutations (Q115002701)
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scientific article published in 2022
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Common variable immunodeficiency in two kindreds with heterogeneous phenotypes caused by novel heterozygous NFKB1 mutations |
scientific article published in 2022 |
Statements
Common variable immunodeficiency in two kindreds with heterogeneous phenotypes caused by novel heterozygous NFKB1 mutations (English)
Frederik Staels
Kerstin De Keukeleere
Matias Kinnunen
Salla Keskitalo
Flaminia Lorenzetti
Michiel Vanmeert
Teresa Prezzemolo
Emanuela Pasciuto
Eveline Lescrinier
Xavier Bossuyt
Margaux Gerbaux
Mathijs Willemsen
Julika Neumann
Sien Van Loo
Anniek Corveleyn
Karen Willekens
Ingeborg Stalmans
Isabelle Meyts
Adrian Liston
Stephanie Humblet-Baron
Mikko Seppänen
Markku Varjosalo
Rik Schrijvers
20 September 2022
13
20 September 2022
1 reference