CFI Gene

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Zhou, V. CFI Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/5118 (accessed on 22 September 2026).

Zhou V. CFI Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/5118. Accessed September 22, 2026.

Zhou, Vicky. "CFI Gene" Encyclopedia, https://encyclopedia.pub/entry/5118 (accessed September 22, 2026).

Zhou, V. (2020, December 24). CFI Gene. In Encyclopedia. https://encyclopedia.pub/entry/5118

Zhou, Vicky. "CFI Gene." Encyclopedia. Web. 24 December, 2020.

CFI Gene

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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/gene/cfi

complement factor I

genes

References

Baracho GV, Nudelman V, Isaac L. Molecular characterization of homozygoushereditary factor I deficiency. Clin Exp Immunol. 2003 Feb;131(2):280-6.
Fagerness JA, Maller JB, Neale BM, Reynolds RC, Daly MJ, Seddon JM. Variation near complement factor I is associated with risk of advanced AMD. Eur J HumGenet. 2009 Jan;17(1):100-4. doi: 10.1038/ejhg.2008.140.
Kavanagh D, Richards A, Noris M, Hauhart R, Liszewski MK, Karpman D, Goodship JA, Fremeaux-Bacchi V, Remuzzi G, Goodship TH, Atkinson JP. Characterization ofmutations in complement factor I (CFI) associated with hemolytic uremic syndrome.Mol Immunol. 2008 Jan;45(1):95-105.
Nilsson SC, Trouw LA, Renault N, Miteva MA, Genel F, Zelazko M, Marquart H,Muller K, Sjöholm AG, Truedsson L, Villoutreix BO, Blom AM. Genetic, molecularand functional analyses of complement factor I deficiency. Eur J Immunol. 2009Jan;39(1):310-23. doi: 10.1002/eji.200838702.
Ponce-Castro IM, González-Rubio C, Delgado-Cerviño EM, Abarrategui-Garrido C, Fontán G, Sánchez-Corral P, López-Trascasa M. Molecular characterization ofComplement Factor I deficiency in two Spanish families. Mol Immunol. 2008May;45(10):2764-71. doi: 10.1016/j.molimm.2008.02.008.
Richard I. The genetic and molecular bases of monogenic disorders affectingproteolytic systems. J Med Genet. 2005 Jul;42(7):529-39. Review.
Servais A, Frémeaux-Bacchi V, Lequintrec M, Salomon R, Blouin J, Knebelmann B,Grünfeld JP, Lesavre P, Noël LH, Fakhouri F. Primary glomerulonephritis withisolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome. J Med Genet. 2007 Mar;44(3):193-9.
Vyse TJ, Morley BJ, Bartok I, Theodoridis EL, Davies KA, Webster AD, WalportMJ. The molecular basis of hereditary complement factor I deficiency. J ClinInvest. 1996 Feb 15;97(4):925-33.
Vyse TJ, Späth PJ, Davies KA, Morley BJ, Philippe P, Athanassiou P, Giles CM, Walport MJ. Hereditary complement factor I deficiency. QJM. 1994Jul;87(7):385-401. Review.

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Subjects: Genetics & Heredity

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