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.
- Trück, J.
- Asgari, S.
- Sancho-Shimizu, V.
- Agyeman, P.K.A.
- Bellos, E.
- Giannoni, E.
- Stocker, M.
- Posfay-Barbe, K.M.
- Heininger, U.
- Bernhard-Stirnemann, S.
- Niederer-Loher, A.
- Kahlert, C.R.
- Natalucci, G.
- Relly, C.
- Riedel, T.
- Kuehni, C.E.
- Thorball, C.W.
- Chaturvedi, N.
- Martinon-Torres, F.
- Kuijpers, T.W.
- Coin, L.
- Wright, V.
- Herberg, J.
- Levin, M.
- Aebi, C.
- Berger, C.
- Fellay, J.
- Schlapbach, L.J.
- Mostrar todos os autores +
ISSN: 1537-6591, 1058-4838
Ano de publicación: 2020
Volume: 71
Número: 10
Páxinas: E614-E623
Tipo: Artigo