ITGB2 mutation combined with deleted ring 21 chromosome in a child with leukocyte adhesion deficiency - 12/08/11
Doi : 10.1016/j.jaci.2009.07.058
Maurilia Fiorini, PhD a, 
, Giovanna Piovani, PhD d, , Richard F. Schumacher, MD b, Chiara Magri, PhD d, Valeria Bertini d, Evelina Mazzolari, MD b, Lucia Notarangelo, MD b, Luigi D. Notarangelo, MD c, e, Sergio Barlati, PhD d 
, Giovanna Piovani, PhD d, , Richard F. Schumacher, MD b, Chiara Magri, PhD d, Valeria Bertini d, Evelina Mazzolari, MD b, Lucia Notarangelo, MD b, Luigi D. Notarangelo, MD c, e, Sergio Barlati, PhD d a “Angelo Nocivelli” Institute for Molecular Medicine, University of Brescia, Italy
b Divisione di Emato-Oncologia Pediatrica, University of Brescia, Italy
c Clinica Pediatrica, Ospedale dei Bambini, Spedali Civili, University of Brescia, Italy
d Biology and Genetics, Department Biomedical Sciences and Biotechnology, University of Brescia, Italy
e Division of Immunology and Manton Center for Orphan Disease Research, Children’s Hospital, Harvard Medical School, Boston, Mass
Le texte complet de cet article est disponible en PDF.
| Supported by Centro di Studio e ricerca sulle malattie Ereditarie and MIUR (to S.B.) and the Manton Foundation (to L.N.). |
|
| Disclosure of potential conflict of interest: L. Notarangelo has received research support from the National Institutes of Health and the Manton Foundation. The rest of the authors have declared that they have no conflict of interest. |
© 2009
American Academy of Allergy, Asthma & Immunology. Publié par Elsevier Masson SAS. Tous droits réservés.
Vol 124 - N° 6
P. 1356-1358 - décembre 2009 Retour au numéro
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