Human immune disorder associated with homozygous hypomorphic mutation affecting MALT1B splice variant - 04/02/21
Doi : 10.1016/j.jaci.2020.07.034
Necil Kutukculer, MD a, ∗ 
, Thomas Seeholzer, MSc b, ∗, Thomas J. O’Neill, MSc b, Carina Graß, MSc b, Ayca Aykut, MD c, Neslihan Edeer Karaca, MD a, Asude Durmaz, MD c, Ozgur Cogulu, MD c, Guzide Aksu, MD a, Torben Gehring, PhD b, Andreas Gewies, PhD b, Daniel Krappmann, PhD b
, Thomas Seeholzer, MSc b, ∗, Thomas J. O’Neill, MSc b, Carina Graß, MSc b, Ayca Aykut, MD c, Neslihan Edeer Karaca, MD a, Asude Durmaz, MD c, Ozgur Cogulu, MD c, Guzide Aksu, MD a, Torben Gehring, PhD b, Andreas Gewies, PhD b, Daniel Krappmann, PhD b a Department of Pediatric Immunology, Ege University Faculty of Medicine, Izmir, Turkey
b Research Unit Cellular Signal Integration, Helmholtz Zentrum München–German Research Center for Environmental Health, Neuherberg, Germany
c Department of Medical Genetics, Ege University Faculty of Medicine, Izmir, Turkey
| Disclosure of potential conflict of interest: D. Krappmann is a consultant for Monopteros Therapeutics, Boston. The rest of the authors declare that they have no relevant conflicts of interest. |
© 2020
American Academy of Allergy, Asthma & Immunology. Publié par Elsevier Masson SAS. Tous droits réservés.
Vol 147 - N° 2
P. 775 - février 2021 Retour au numéro
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