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Zhou, V. AMN Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/4671 (accessed on 28 September 2026).
Zhou V. AMN Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/4671. Accessed September 28, 2026.
Zhou, Vicky. "AMN Gene" Encyclopedia, https://encyclopedia.pub/entry/4671 (accessed September 28, 2026).
Zhou, V. (2020, December 24). AMN Gene. In Encyclopedia. https://encyclopedia.pub/entry/4671
Zhou, Vicky. "AMN Gene." Encyclopedia. Web. 24 December, 2020.
AMN Gene
Edit

amnion associated transmembrane protein

genes

References

  1. Beech CM, Liyanarachchi S, Shah NP, Sturm AC, Sadiq MF, de la Chapelle A,Tanner SM. Ancient founder mutation is responsible for Imerslund-GräsbeckSyndrome among diverse ethnicities. Orphanet J Rare Dis. 2011 Nov 13;6:74. doi:10.1186/1750-1172-6-74.
  2. Fyfe JC, Madsen M, Højrup P, Christensen EI, Tanner SM, de la Chapelle A, HeQ, Moestrup SK. The functional cobalamin (vitamin B12)-intrinsic factor receptor is a novel complex of cubilin and amnionless. Blood. 2004 Mar 1;103(5):1573-9.
  3. Kozyraki R, Cases O. Vitamin B12 absorption: mammalian physiology and acquiredand inherited disorders. Biochimie. 2013 May;95(5):1002-7. doi:10.1016/j.biochi.2012.11.004.
  4. Namour F, Dobrovoljski G, Chery C, Audonnet S, Feillet F, Sperl W, Gueant JL. Luminal expression of cubilin is impaired in Imerslund-Grasbeck syndrome withcompound AMN mutations in intron 3 and exon 7. Haematologica. 2011Nov;96(11):1715-9. doi: 10.3324/haematol.2011.043984.
  5. Watkins D, Rosenblatt DS. Lessons in biology from patients with inborn errors of vitamin B12 metabolism. Biochimie. 2013 May;95(5):1019-22. doi:10.1016/j.biochi.2013.01.013.
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Update Date: 24 Dec 2020
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