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A novel form of cell type-specific partial IFN-gamma R1 deficiency caused by a germ line mutation of the IFNGR1 initiation codon

Kong, X-F; Vogt, G; Chapgier, A; Lamaze, C; Bustamante, J; Prando, C; Fortin, A; ... Casanova, J-L; + view all (2010) A novel form of cell type-specific partial IFN-gamma R1 deficiency caused by a germ line mutation of the IFNGR1 initiation codon. HUMAN MOLECULAR GENETICS , 19 (3) pp. 434-444. 10.1093/hmg/ddp507.

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Type: Article
Title: A novel form of cell type-specific partial IFN-gamma R1 deficiency caused by a germ line mutation of the IFNGR1 initiation codon
DOI: 10.1093/hmg/ddp507
Keywords: Science & Technology, Life Sciences & Biomedicine, Biochemistry & Molecular Biology, Genetics & Heredity, INTERFERON-GAMMA-RECEPTOR, BACILLE CALMETTE-GUERIN, INHERITED INTERLEUKIN-12 DEFICIENCY, SMALL DELETION HOTSPOT, MYCOBACTERIAL INFECTION, INTERFERON-GAMMA-RECEPTOR-1 DEFICIENCY, CLINICAL-FEATURES, MEDIATED IMMUNITY, STAT1 DEFICIENCY, AVIUM INFECTION
UCL classification: UCL > Provost and Vice Provost Offices
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences > Cancer Institute
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences > Cancer Institute > Research Department of Haematology
URI: http://discovery.ucl.ac.uk/id/eprint/1356233
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