Heterozygous Mutations in NFKB2 Exhibit a Broad Clinical Phenotype - 28/02/18
Doi : 10.1016/j.jaci.2017.12.065
Erik N. Newman 1, Julie Feusier 1, Shancy P. Jacob 1, Lynn B. Jorde 1, Harry R. Hill 1, 2, Celine Hanson 3, Kazushi Izawa 4, T. Ronan Leahy 5, Masafumi Yamada 6, William Rae 7, Fabian Hauck 8, Hassan Abolhassani 9, Asghar Aghamohammadi 9, Lennart Hammarström 10, Hirokazu Kanegane 11, Charlotte Slade 12, Chaim M. Roifman 13, Bodo Grimbacher 14, Guy A. Zimmerman 1, John F. Bohnsack 1, Karin Chen 1
1 University of Utah, Salt Lake City, UT
2 ARUP Institute for Clinical and Experimental Pathology, Salt Lake City, UT
3 Texas Children's Hospital, Houston, TX
4 Kyoto University Graduate School of Medicine, Kyoto, Japan
5 Our Lady’s Children’s Hospital, Dublin, Ireland
6 Hokkaido University, Sapporo, Japan
7 University Hospital Southampton NHSFT, Southampton, United Kingdom
8 Dr von Hauner Children's Hospital, Ludwig-Maximilians-Universität, Munich, Germany
9 Children Medical Center Hospital, Tehran University of Medical Sciences, Tehran, Iran (Islamic Republic of)
10 Karolinska University Hospital, Stockholm, Sweden
11 Tokyo Medical and Dental University, Tokyo, Japan
12 Royal Melbourne Hospital, Melbourne, Australia
13 The Hospital for Sick Children and the University of Toronto, Toronto, Canada
14 University of Freiburg, Freiburg, Germany
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© 2017
Publié par Elsevier Masson SAS.
Vol 141 - N° 2S
P. AB21 - février 2018 Retour au numéro
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