Whole-exome sequencing for the identification of rare variants in primary immunodeficiency genes in children with sepsis - a prospective population-based cohort study
Borghesi A, Kuehni C, Thorball C, Chaturvedi N, Martinon-Torres F, Kuijpers T, Coin L, Wright V, Herberg J, Levin M, Aebi C, Christoph B, Fellay J, Schlapbach L, Riedel T, Relly C, Trück J, Asgari S, Sancho-Shimizu V, Agyeman P, Bellos E, Giannoni E, Stocker M, Posfay-Barbe K, Heininger U, Bernhard-Stirnemann S, Niederer-Loher A, Kahlert C, Natalucci G, EUCLIDS consortium and the Swiss Paediatric Sepsis Study. Whole-exome sequencing for the identification of rare variants in primary immunodeficiency genes in children with sepsis - a prospective population-based cohort study. Clin Infect Dis 2020
18.03.2020
Whole-exome sequencing for the identification of rare variants in primary immunodeficiency genes in children with sepsis - a prospective population-based cohort study
18.03.2020
Clin Infect Dis 2020
Borghesi Alessandro, Kuehni Claudia E, Thorball Christian W, Chaturvedi Nimisha, Martinon-Torres Federico, Kuijpers Taco W, Coin Lachlan, Wright Victoria, Herberg Jethro, Levin Michael, Aebi Christoph, Christoph Berger, Fellay Jacques, Schlapbach Luregn J, Riedel Thomas, Relly Christa, Trück Johannes, Asgari Samira, Sancho-Shimizu Vanessa, Agyeman Philipp K A, Bellos Evangelos, Giannoni Eric, Stocker Martin, Posfay-Barbe Klara M, Heininger Ulrich, Bernhard-Stirnemann Sara, Niederer-Loher Anita, Kahlert Christian, Natalucci Giancardlo, EUCLIDS consortium and the Swiss Paediatric Sepsis Study
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