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). |
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| 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. Publicado por Elsevier Masson SAS. Todos los derechos reservados.
Vol 138 - N° 6
P. 1706 - décembre 2016 Regresar al número
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