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Corrigendum: Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Front Immunol
Prif Awduron: Cifaldi, Cristina, Brigida, Immacolata, Barzaghi, Federica, Zoccolillo, Matteo, Ferradini, Valentina, Petricone, Davide, Cicalese, Maria Pia, Lazarevic, Dejan, Cittaro, Davide, Omrani, Maryam, Attardi, Enrico, Conti, Francesca, Scarselli, Alessia, Chiriaco, Maria, Di Cesare, Silvia, Licciardi, Francesco, Davide, Montin, Ferrua, Francesca, Canessa, Clementina, Pignata, Claudio, Giliani, Silvia, Ferrari, Simona, Fousteri, Georgia, Barera, Graziano, Merli, Pietro, Palma, Paolo, Cesaro, Simone, Gattorno, Marco, Trizzino, Antonio, Moschese, Viviana, Chini, Loredana, Villa, Anna, Azzari, Chiara, Finocchi, Andrea, Locatelli, Franco, Rossi, Paolo, Sangiuolo, Federica, Aiuti, Alessandro, Cancrini, Caterina, Di Matteo, Gigliola
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Frontiers Media S.A. 2019
Pynciau:
Immunology
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC6554535/
https://ncbi.nlm.nih.gov/pubmed/31214169
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fimmu.2019.01184
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  • Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies
    gan: Cifaldi, Cristina, et al.
    Cyhoeddwyd: (2019)
  • First Case of Patient With Two Homozygous Mutations in MYD88 and CARD9 Genes Presenting With Pyogenic Bacterial Infections, Elevated IgE, and Persistent EBV Viremia
    gan: Chiriaco, Maria, et al.
    Cyhoeddwyd: (2019)
  • JAK3 mutations in Italian patients affected by SCID: New molecular aspects of a long‐known gene
    gan: Di Matteo, Gigliola, et al.
    Cyhoeddwyd: (2018)
  • Novel X-Linked Inhibitor of Apoptosis Mutation in Very Early-Onset Inflammatory Bowel Disease Child Successfully Treated with HLA-Haploidentical Hemapoietic Stem Cells Transplant after Removal of αβ(+) T and B Cells
    gan: Cifaldi, Cristina, et al.
    Cyhoeddwyd: (2017)
  • Urogenital Abnormalities in Adenosine Deaminase Deficiency
    gan: Pajno, Roberta, et al.
    Cyhoeddwyd: (2020)

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