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. 1993 Mar 20;306(6880):794–795. doi: 10.1136/bmj.306.6880.794-c

Inherited prion disease.

J L Laplanche, J Chatelain, M Dussaucy, C Bounneau, J M Launay, J P Brandel, N Delasnerie-Laupretre
PMCID: PMC1677204  PMID: 8490359

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Baker H. E., Poulter M., Crow T. J., Frith C. D., Lofthouse R., Ridley R. M. Aminoacid polymorphism in human prion protein and age at death in inherited prion disease. Lancet. 1991 May 25;337(8752):1286–1286. doi: 10.1016/0140-6736(91)92953-y. [DOI] [PubMed] [Google Scholar]
  2. Collinge J., Palmer M. S., Campbell T., Sidle K. C., Carroll D., Harding A. Inherited prion disease (PrP lysine 200) in Britain: two case reports. BMJ. 1993 Jan 30;306(6873):301–302. doi: 10.1136/bmj.306.6873.301. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Goldfarb L. G., Petersen R. B., Tabaton M., Brown P., LeBlanc A. C., Montagna P., Cortelli P., Julien J., Vital C., Pendelbury W. W. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism. Science. 1992 Oct 30;258(5083):806–808. doi: 10.1126/science.1439789. [DOI] [PubMed] [Google Scholar]

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