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  1. 1.   Inherited p40(phox) deficiency differs from classic chronic granulomatous disease
  2. van de Geer, Annemarie; Nieto-Patlan, Alejandro; Kuhns, Doug; Tool, Anton T. J.; Arias, Andres A.; Bouaziz, Matthieu; de Boer, Martin; Luis Franco, Jose; Gazendam, Roel P.; van Hamme, John L.; van Houdt, Michel; van Leeuwen, Karin; Verkuijlen, Paul J. H.; van den Berg, Timo K.; Alzate, Juan F.; Arango-Franco, Carlos A.; Batura, Vritika; Bernasconi, Andrea R.; Boardman, Barbara; Booth, Claire; Burns, Siobhan O.; Cabarcas, Felipe; Bensussan, Nadine Cerf; Charbit-Henrion, Fabienne; Corveleyn, Anniek; Deswarte, Caroline; Esnaola Azcoiti, Maria; Foell, Dirk; Gallin, John I.; Garces, Carlos; Guedes, Margarida; Hinze, Claas H.; Holland, Steven M.; Hughes, Stephen M.; Ibanez, Patricio; Malech, Harry L.; Meyts, Isabelle; Moncada-Velez, Marcela; Moriya, Kunihiko; Neves, Esmeralda; Oleastro, Matias; Perez, Laura; Rattina, Vimel; Oleaga-Quintas, Carmen; Warner, Neil; Muise, Aleixo M.; Serafin Lopez, Jeanet; Trindade, Eunice; Vasconcelos, Julia; Vermeire, Severine; Wittkowski, Helmut; Worth, Austen; Abel, Laurent; Dinauer, Mary C.; Arkwright, Peter D.; Roos, Dirk; Casanova, Jean-Laurent; Kuijpers, Taco W.; Bustamante, Jacinta
  3. Journal of Clinical Investigation. 2018, Aug 31; 128(9): 3957-3975.
  1. 2.   Correction of X-linked chronic granulomatous disease by gene therapy, augmented by insertional activation of MDS1-EVI1, PRDM16 or SETBP1
  2. Ott, M. G.; Schmidt, M.; Schwarzwaelder, K.; Stein, S.; Siler, U.; Koehl, U.; Glimm, H.; Kuhlcke, K.; Schilz, A.; Kunkel, H.; Naundorf, S.; Brinkmann, A.; Deichmann, A.; Fischer, M.; Ball, C.; Pilz, I.; Dunbar, C.; Du, Y.; Jenkins, N. A.; Copeland, N. G.; Luthi, U.; Hassan, M.; Thrasher, A. J.; Hoelzer, D.; von Kalle, C.; Seger, R.; Grez, M.
  3. Nature Medicine. 2006, Apr; 12(4): 401-409.
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