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      <title><![CDATA[Aschenbrenner, D.* et al. Pathogenic interleukin-10 receptor alpha variants in humans - balancing natural selection and clinical implications. J. Clin. Immunol., DOI: 10.1007/s10875-022-01366-7 (2022)]]></title>
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      <title><![CDATA[Schwierzeck, V. et al. Molecular assessment of Staphylococcus Aureus strains in STAT3 Hyper-IgE syndrome patients. J. Clin. Immunol. 42, 1301-1309 (2022)]]></title>
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      <pubDate>Sat, 18 Jun 2022 00:00:00 +0000</pubDate>
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      <title><![CDATA[Sefer, A.P.* et al. Expanding the clinical and immunological phenotypes and natural history of MALT1 deficiency. J. Clin. Immunol. 42, 634-652 (2022)]]></title>
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      <pubDate>Wed, 08 Jun 2022 00:00:00 +0000</pubDate>
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      <title><![CDATA[Lenz, D.* et al. NBAS variants are associated with quantitative and qualitative NK and B cell deficiency. J. Clin. Immunol., DOI: 10.1007/s10875-021-01110-7 (2021)]]></title>
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      <title><![CDATA[Daschkey, S.* et al. Fatal lymphoproliferative disease in two siblings lacking functional FAAP24. J. Clin. Immunol. 36, 684-692 (2016)]]></title>
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      <pubDate>Mon, 01 Aug 2016 00:00:00 +0000</pubDate>
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      <title><![CDATA[Poeck, H.* &amp; Ruland, J. ITAM receptor signaling and the NLRP3 inflammasome in antifungal immunity. J. Clin. Immunol. 30, 496-501 (2010)]]></title>
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      <title><![CDATA[Hügle, B.* et al. Persistent hypogammaglobulinemia following mononucleosis in boys is highly suggestive of X-linked lymphoproliferative disease--report of three cases. J. Clin. Immunol. 24, 515-522 (2005)]]></title>
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      <pubDate>Tue, 13 Dec 2005 00:00:00 +0000</pubDate>
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