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- databases for immunodeficiency-causing variations

   FOXN1base
   Variation registry for  T-cell immunodeficiency, congenital alopecia, and nail dystrophy


FOXN1base mutation publications

[2001] [1999] [1996]

Search PubMed latest citations for FOXN1 mutations

    2001

  • Human equivalent of the mouse Nude/SCID phenotype: long-term evaluation of immunologic reconstitution after bone marrow transplantation.
    Pignata C, Gaetaniello L, Masci AM, Frank J, Christiano A, Matrecano E, Racioppi L
    Blood 2001(4): 880-5 [PubMed abstract].

    1999

  • Exposing the human nude phenotype.
    Frank J, Pignata C, Panteleyev AA, Prowse DM, Baden H, Weiner L, Gaetaniello L, Ahmad W, Pozzi N, Cserhalmi-Friedman PB, Aita VM, Uyttendaele H, Gordon D, Ott J, Brissette JL, Christiano AM
    Nature 1999(6727): 473-4 [PubMed abstract].

    1996

  • Congenital Alopecia and nail dystrophy associated with severe functional T-cell immunodeficiency in two sibs.
    Pignata C, Fiore M, Guzzetta V, Castaldo A, Sebastio G, Porta F, Guarino A
    Am J Med Genet 1996(2): 167-70 [PubMed abstract].