New human combined immunodeficiency caused by interferon regulatory factor 4 (IRF4) deficiency inherited by uniparental isodisomy - 04/05/18
![](/templates/common/images/mail.png)
A.B.M. received a fellowship from the Spanish MINECO (SVP-2014-068263). A.J.-R. was supported by the MINECO (FPI BES-2012-055054). A.V.M. was supported by the Comunidad de Madrid (CAM S2010/BMD-2316) and the Complutense University (CT46/15-Harvard Univ). A.B.C. was supported by the Complutense University (CT28/16). P.C. was supported by the MINECO (152JA19262). This work was supported by grants from the Spanish Association Against Cancer (AECC) and Carlos III Health Institute PI16/01605) to E.L.-G. and the MINECO SAF2014-58752-R to H.T.R., SAF2015-69169-R to M.V.G., and SAF2014-54708-R to J.R.R.). |
|
Disclosure of potential conflict of interest: A. Blázquez Moreno's institution has received grant funding from MINEICO (SVP-2014-068263). A. del Pozo Maté has received consultancy fees from ENAC and lecture fees from the Health Institute Carlos III. E. Vallespín García has received funds for expert testimony for the Scienceboard.net and royalties from KARYOARRAY-8.512.907. M. Valés-Gómez's institution has received grant funding from MINEICO (SAF2015-69169-R) and Comunidad de Madrid (S2010/BMD-2326). H. T. Reyburn's institution has received a grant from MINEICO (SAF2014-58752-R). The rest of the authors declare that they have no relevant conflicts of interest. |
Vol 141 - N° 5
P. 1924 - mai 2018 Retour au numéroBienvenue 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 ?