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Li, V. FOXN1 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/5581 (accessed on 21 September 2026).
Li V. FOXN1 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/5581. Accessed September 21, 2026.
Li, Vivi. "FOXN1 Gene" Encyclopedia, https://encyclopedia.pub/entry/5581 (accessed September 21, 2026).
Li, V. (2020, December 25). FOXN1 Gene. In Encyclopedia. https://encyclopedia.pub/entry/5581
Li, Vivi. "FOXN1 Gene." Encyclopedia. Web. 25 December, 2020.
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Forkhead box N1
genes
References
- Adriani M, Martinez-Mir A, Fusco F, Busiello R, Frank J, Telese S, MatrecanoE, Ursini MV, Christiano AM, Pignata C. Ancestral founder mutation of the nude(FOXN1) gene in congenital severe combined immunodeficiency associated withalopecia in southern Italy population. Ann Hum Genet. 2004 May;68(Pt 3):265-8.
- Amorosi S, D'Armiento M, Calcagno G, Russo I, Adriani M, Christiano AM, WeinerL, Brissette JL, Pignata C. FOXN1 homozygous mutation associated with anencephalyand severe neural tube defect in human athymic Nude/SCID fetus. Clin Genet. 2008 Apr;73(4):380-4. doi: 10.1111/j.1399-0004.2008.00977.x.
- Amorosi S, Vigliano I, Del Giudice E, Panico L, Maruotti GM, Fusco A,Quarantelli M, Ciccone C, Ursini MV, Martinelli P, Pignata C. Brain alteration ina Nude/SCID fetus carrying FOXN1 homozygous mutation. J Neurol Sci. 2010 Nov15;298(1-2):121-3. doi: 10.1016/j.jns.2010.08.066.
- Pignata C, Fusco A, Amorosi S. Human clinical phenotype associated with FOXN1 mutations. Adv Exp Med Biol. 2009;665:195-206. Review.
- Pignata C. A lesson for unraveling complex aspects of novel immunodeficienciesfrom the human equivalent of the nude/SCID phenotype. J Hematother Stem Cell Res.2002 Apr;11(2):409-14. Review.
- Vigliano I, Gorrese M, Fusco A, Vitiello L, Amorosi S, Panico L, Ursini MV,Calcagno G, Racioppi L, Del Vecchio L, Pignata C. FOXN1 mutation abrogatesprenatal T-cell development in humans. J Med Genet. 2011 Jun;48(6):413-6. doi:10.1136/jmg.2011.089532.
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