Ectodermal dysplasia with immunodeficiency caused by a branch-point mutation in IKBKG/NEMO - 18/04/17
Doi : 10.1016/j.jaci.2016.05.030
Sofie E. Jørgensen, MS a, ∗, Pernille Bøttger, PhD b, ∗, Emil Kofod-Olsen, PhD b, Mette Holm, MD, PhD b, c, Nanna Mørk, MD a, Torben F. Ørntoft, MD, PhD d, Uffe B.S. Sørensen, PhD e, Jens Magnus Bernth-Jensen, MD b, f, Troels Herlin, MD, DMSc b, c, Jens Veirum, MD, PhD b, c, Carsten S. Larsen, MD, DMSc a, b, Lars Østergaard, MD, DMSc a, b, Rune Hartmann, PhD g, h, Mette Christiansen, PhD b, f, Trine H. Mogensen, MD, PhD, DMSc a, b, e, h 
a Department of Infectious Diseases, Aarhus University Hospital Skejby, Aarhus, Denmark
b International Center for Immunodeficiency Diseases, Aarhus University Hospital Skejby, Aarhus, Denmark
c Department of Pediatrics, Aarhus University Hospital Skejby, Aarhus, Denmark
d Department of Molecular Medicine, Aarhus University Hospital Skejby, Aarhus, Denmark
e Department of Biomedicine, Aarhus University, Aarhus, Denmark
f Department of Clinical Immunology, Aarhus University Hospital Skejby, Aarhus, Denmark
g Department of Molecular Biology and Genetics, Aarhus University, Aarhus, Denmark
h Aarhus Research Center for Innate Immunity, Aarhus University, Aarhus, Denmark
| The work was supported by the Lundbeck Foundation (grant no. R151-2013-14668) and the Danish Research Council (grant no. #DFF – 4004-00047). |
|
| Disclosure of potential conflict of interest: S. E. Jørgensen and N. Moerk receive support from the Lundbeck Foundation. T. H. Mogensen receives research support from the DK Research council. The rest of the authors declare that they have no relevant conflicts of interest. |
© 2016
American Academy of Allergy, Asthma & Immunology. Publié par Elsevier Masson SAS. Tous droits réservés.
Vol 138 - N° 6
P. 1706 - décembre 2016 Retour au numéro
Article précédent
- Early-life ozone exposure associated with asthma without sensitization in Latino children
- Katherine K. Nishimura, Kensho Iwanaga, Sam S. Oh, Maria Pino-Yanes, Celeste Eng, Anjeni Keswani, Lindsey A. Roth, Elizabeth A. Nguyen, Shannon M. Thyne, Harold J. Farber, Denise Serebrisky, Kelley Meade, Michael A. LeNoir, William Rodriguez-Cintron, Luisa N. Borrell, Kirsten Bibbins-Domingo, Fred Lurmann, ?aunak Sen, Jose R. Rodriguez-Santana, Emerita Brigino-Buenaventura, Pedro C. Avila, John R. Balmes, Rajesh Kumar, Esteban G. Burchard
- Complete human CD1a deficiency on Langerhans cells due to a rare point mutation in the coding sequence
- Daniela Cerny, Duyen Huynh Thi Le, Trung Dinh The, Roland Zuest, Srinivasan KG, Sumathy Velumani, Chiea Chuen Khor, Lucia Mori, Cameron P. Simmons, Michael Poidinger, Francesca Zolezzi, Florent Ginhoux, Muzlifah Haniffa, Bridget Wills, Katja Fink
Bienvenue sur EM-consulte, la référence des professionnels de santé.
L’accès au texte intégral de cet article nécessite un abonnement.
Déjà abonné à cette revue ?