Human ClinicalPhenotype Associated with FOXN1 Mutations
Author:
Publisher
Springer New York
Link
http://link.springer.com/content/pdf/10.1007/978-1-4419-1599-3_15.pdf
Reference84 articles.
1. Bonilla FA, Geha RS. Primary immunodeficiency diseases. J Allergy Clin Immunol 2003; 111:S571–581.
2. Pignata C, Fiore M, Guzzetta V et al. Congenital Alopecia and nail dystrophy associated with severe functional T-cell immunodeficiency in two sibs. Am J Med Genet 1996; 65:167–170.
3. Pignata C. A lesson to unraveling complex aspects of novel immunodeficiencies from the human equivalent of the nude/SCID phenotype. Journal of Hematotherapy and Stem Cell Research 2002; 11:409–414.
4. Flanagan SP. ‘Nude’, a new hairless gene with pleiotropic effects in the mouse. Genet Res 1966; 8:295–309.
5. Schlake T. The nude gene and the skin. Exp Dermatol 2001; 10:293–304.
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