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Whole-exome Sequencing for the Identification of Rare Varia..:
Borghesi, Alessandro
;
Trück, Johannes
;
Asgari, Samira
...
Clinical Infectious Diseases. 71 (2020) 10 - p. e614-e623 , 2020
Link:
https://doi.org/10.1093/cid/ciaa290
RT Journal T1
Whole-exome Sequencing for the Identification of Rare Variants in Primary Immunodeficiency Genes in Children With Sepsis: A Prospective, Population-based Cohort Study
UL https://suche.suub.uni-bremen.de/peid=cr-10.1093_cid_ciaa290&Exemplar=1&LAN=DE A1 Borghesi, Alessandro A1 Trück, Johannes A1 Asgari, Samira A1 Sancho-Shimizu, Vanessa A1 Agyeman, Philipp K A A1 Bellos, Evangelos A1 Giannoni, Eric A1 Stocker, Martin A1 Posfay-Barbe, Klara M A1 Heininger, Ulrich A1 Bernhard-Stirnemann, Sara A1 Niederer-Loher, Anita A1 Kahlert, Christian R A1 Natalucci, Giancarlo A1 Relly, Christa A1 Riedel, Thomas A1 Kuehni, Claudia E A1 Thorball, Christian W A1 Chaturvedi, Nimisha A1 Martinon-Torres, Federico A1 Kuijpers, Taco W A1 Coin, Lachlan A1 Wright, Victoria A1 Herberg, Jethro A1 Levin, Michael A1 Aebi, Christoph A1 Berger, Christoph A1 Fellay, Jacques A1 Schlapbach, Luregn J PB Oxford University Press (OUP) YR 2020 SN 1058-4838 SN 1537-6591 JF Clinical Infectious Diseases VO 71 IS 10 SP e614 OP e623 LK http://dx.doi.org/https://doi.org/10.1093/cid/ciaa290 DO https://doi.org/10.1093/cid/ciaa290 SF ELIB - SuUB Bremen
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