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  • Expanding the mutation spec... Expanding the mutation spectrum in ICF syndrome: Evidence for a gender bias in ICF2
    van den Boogaard, M.L.; Thijssen, P.E.; Aytekin, C. ... Clinical genetics, October 2017, Volume: 92, Issue: 4
    Journal Article
    Peer reviewed

    Background Immunodeficiency, centromeric instability, and facial anomalies (ICF) syndrome is a rare, genetically heterogeneous, autosomal recessive disorder. Patients suffer from recurrent infections ...
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  • Recommendations for care, prevention of infections and chemoprophylaxis in inborn errors of immunity
    Villa, Mariana; Merhar, Claudia; Nievas, Elma ... Archivos argentinos de pediatría, 02/2023, Volume: 121, Issue: 1
    Journal Article
    Peer reviewed

    Inborn errors of immunity, previously named primary immunodeficiency are a heterogeneous group of genetic defects of different components of the immune system. Patients present high susceptibility to ...
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