Common variable immunodeficiency in two kindreds with heterogeneous phenotypes caused by novel heterozygous NFKB1 mutations
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M. Varjosalo | A. Liston | Flaminia C Lorenzetti | A. Corveleyn | S. Keskitalo | Michiel Vanmeert | I. Meyts | X. Bossuyt | R. Schrijvers | I. Stalmans | E. Lescrinier | S. Humblet-Baron | K. Willekens | E. Pasciuto | F. Staels | T. Prezzemolo | Julika Neumann | M. Gerbaux | M. Willemsen | Matias Kinnunen | M. Seppänen | Kerstin De Keukeleere | S. Van Loo | Emanuela Pasciuto
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