| 1 | NCF1, NCF1D
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| Chronic granulomatous disease: Clinical, molecular, and therapeutic aspects.
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| Chiriaco M, Salfa I, Di Matteo G, Rossi P, Finocchi A.
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| Pediatr Allergy Immunol 27(3):242-53. doi: 10.1111/pai.12527. Review.
2016
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| 2 | NCF1, NCF1D
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| Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (second update).
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| Roos D, Kuhns DB, Maddalena A, Bustamante J, Kannengiesser C, de Boer M, van Leeuwen K, Köker MY, Wolach B, Roesler J, Malech HL, Holland SM, Gallin JI, Stasia MJ.
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| Blood Cells Mol Dis 44(4):291-9. Epub 2010 Feb 18. Review.PMID: 20167518 2010
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| 3 | NCF1, NCF1D
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| A novel mutation in NCF1 in an adult CGD patient with a liver abscess as first presentation.
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| van de Vosse E, van Wengen A, van Geelen JA, de Boer M, Roos D, van Dissel JT.
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| J Hum Genet 54(6):313-6. Epub 2009 Mar 27.PMID: 19329991 2009
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| 4 | NCF1, NCF1D
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| Autosomal recessive chronic granulomatous disease, IgA deficiency and refractory autoimmune thrombocytopenia responding to Anti-CD20 monoclonal antibody.
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| Shamsian BS, Mansouri D, Pourpak Z, Rezaei N, Chavoshzadeh Z, Jadali F, Gharib A, Alavi S, Eghbali A, Arzanian MT.
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| Iran J Allergy Asthma Immunol 7(3):181-4.PMID: 18780954 2008
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