Whole-exome Sequencing for the Identification of Rare Variants in Primary Immunodeficiency Genes in Children With Sepsis: A Prospective, Population-based Cohort Study

A. Borghesi(Inserm), Luregn J. Schlapbach(The University of Queensland), Claudia E. Kuehni(University of Bern), Nimisha Chaturvedi(Alstom (France)), Taco W. Kuijpers(Sanquin), Christoph Berger(University Children's Hospital Zurich), Philipp Agyeman(University Hospital of Bern), Klara M. Posfay‐Barbe(University Hospital of Geneva), Vanessa Sancho‐Shimizu(Imperial College London), Ulrich Heininger(University Children’s Hospital Basel), Anita Niederer-Loher(Ostschweizer Kinderspital), Evangelos Bellos(Imperial College London), Christa Relly(University Children's Hospital Zurich), Giancarlo Natalucci(University Children's Hospital Zurich), Lachlan Coin(The University of Melbourne), Sara Bernhard‐Stirnemann(Kantonsspital Aarau), Victoria Wright(Wellcome Trust), Christian R. Kahlert(Ostschweizer Kinderspital), Federico Martinón‐Torres(Complejo Hospitalario Universitario de Santiago), Christian W. Thorball(École Polytechnique Fédérale de Lausanne), Jethro Herberg(Imperial College London), Thomas Riedel(German Center for Infection Research), Christoph Aebi(University Hospital of Bern), Johannes Trück(University of Zurich), Samira Asgari(Icahn School of Medicine at Mount Sinai), Jacques Fellay(SIB Swiss Institute of Bioinformatics), Éric Giannoni(University of Lausanne), Michael Levin(University of Chicago), Martin Stocker(University of Lucerne)
Clinical Infectious Diseases
March 15, 2020
Cited by 33


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