Articles

Selective loss of function variants in IL6ST cause Hyper-IgE syndrome with distinct impairments of T-cell phenotype and function

Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria;CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria
Translational Gastroenterology Unit, John Radcliffe Hospital, University of Oxford, UK
Section of Pediatric Immunology, Ihsan Doğramacı Children’s Hospital, Hacettepe University, Ankara, Turkey;Institute of Child Health, Hacettepe University, Ankara, Turkey
Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria;CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria;Department of Pediatric Allergy and Immunology, Ankara University School of Medicine, Cebeci, Turkey
Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria;CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria
Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria;CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria
Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria;CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria
Translational Gastroenterology Unit, John Radcliffe Hospital, University of Oxford, UK;Dr. von Hauner Children’s Hospital, Ludwig-Maximilians-University of Munich, Germany
Section of Pediatric Immunology, Ihsan Doğramacı Children’s Hospital, Hacettepe University, Ankara, Turkey
Section of Pediatric Immunology, Ihsan Doğramacı Children’s Hospital, Hacettepe University, Ankara, Turkey
Section of Pediatric Immunology, Ihsan Doğramacı Children’s Hospital, Hacettepe University, Ankara, Turkey
Clinical Genetics Group, MRC Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, UK
Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, UK
Clinical Genetics Group, MRC Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, UK
Section of Pediatric Immunology, Ihsan Doğramacı Children’s Hospital, Hacettepe University, Ankara, Turkey;Institute of Child Health, Hacettepe University, Ankara, Turkey
Translational Gastroenterology Unit, John Radcliffe Hospital, University of Oxford, UK;Department of Paediatrics, University of Oxford, UK
Ludwig Boltzmann Institute for Rare and Undiagnosed Diseases, Vienna, Austria;CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria;Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Austria;St. Anna Kinderspital and Children’s Cancer Research Institute, Department of Pediatrics, Medical University of Vienna, Austria
Vol. 104 No. 3 (2019): March, 2019 https://doi.org/10.3324/haematol.2018.194233