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Tang, P. PRNP Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/6006 (accessed on 20 September 2026).
Tang P. PRNP Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/6006. Accessed September 20, 2026.
Tang, Peter. "PRNP Gene" Encyclopedia, https://encyclopedia.pub/entry/6006 (accessed September 20, 2026).
Tang, P. (2021, January 04). PRNP Gene. In Encyclopedia. https://encyclopedia.pub/entry/6006
Tang, Peter. "PRNP Gene." Encyclopedia. Web. 04 January, 2021.
PRNP Gene
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Prion protein

genes

References

  1. Caughey B, Baron GS. Prions and their partners in crime. Nature. 2006 Oct19;443(7113):803-10. Review. Citation on PubMed
  2. Collinge J. Molecular neurology of prion disease. J Neurol NeurosurgPsychiatry. 2005 Jul;76(7):906-19. Review. Citation on PubMed or Free article on PubMed Central
  3. Grubenbecher S, Stüve O, Hefter H, Korth C. Prion protein gene codon 129modulates clinical course of neurological Wilson disease. Neuroreport. 2006 Apr3;17(5):549-52. Citation on PubMed
  4. Harris DA, True HL. New insights into prion structure and toxicity. Neuron.2006 May 4;50(3):353-7. Review. Citation on PubMed
  5. Imran M, Mahmood S. An overview of human prion diseases. Virol J. 2011 Dec24;8:559. doi: 10.1186/1743-422X-8-559. Review. Citation on PubMed or Free article on PubMed Central
  6. Merle U, Stremmel W, Gessner R. Influence of homozygosity for methionine atcodon 129 of the human prion gene on the onset of neurological and hepaticsymptoms in Wilson disease. Arch Neurol. 2006 Jul;63(7):982-5. Citation on PubMed
  7. Moore RC, Xiang F, Monaghan J, Han D, Zhang Z, Edström L, Anvret M, PrusinerSB. Huntington disease phenocopy is a familial prion disease. Am J Hum Genet.2001 Dec;69(6):1385-8. Epub 2001 Oct 9. Citation on PubMed or Free article on PubMed Central
  8. Papassotiropoulos A, Wollmer MA, Aguzzi A, Hock C, Nitsch RM, de Quervain DJ. The prion gene is associated with human long-term memory. Hum Mol Genet. 2005 Aug1;14(15):2241-6. Epub 2005 Jun 29. Citation on PubMed
  9. Paucar M, Xiang F, Moore R, Walker R, Winnberg E, Svenningsson P.Genotype-phenotype analysis in inherited prion disease with eight octapeptiderepeat insertional mutation. Prion. 2013 Nov-Dec;7(6):501-10. Epub 2013 Nov 25. Citation on PubMed or Free article on PubMed Central
  10. Perez VP, Coitinho AS. Implications of prion protein biology. Curr NeurovascRes. 2006 Aug;3(3):215-23. Review. Citation on PubMed
  11. Prusiner SB. Shattuck lecture--neurodegenerative diseases and prions. N Engl JMed. 2001 May 17;344(20):1516-26. Review. Citation on PubMed
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Update Date: 04 Jan 2021
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