Literature DB >> 8490359

Inherited prion disease.

J L Laplanche, J Chatelain, M Dussaucy, C Bounneau, J M Launay, J P Brandel, N Delasnerie-Laupretre.   

Abstract

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Year:  1993        PMID： 8490359      PMCID： PMC1677204          DOI： 10.1136/bmj.306.6880.794-c

Source DB:  PubMed          Journal:  BMJ        ISSN： 0959-8138


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  3 in total

1.  Aminoacid polymorphism in human prion protein and age at death in inherited prion disease.

Authors:  H E Baker; M Poulter; T J Crow; C D Frith; R Lofthouse; R M Ridley
Journal:  Lancet       Date:  1991-05-25       Impact factor: 79.321

2.  Inherited prion disease (PrP lysine 200) in Britain: two case reports.

Authors:  J Collinge; M S Palmer; T Campbell; K C Sidle; D Carroll; A Harding
Journal:  BMJ       Date:  1993-01-30

3.  Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism.

Authors:  L G Goldfarb; R B Petersen; M Tabaton; P Brown; A C LeBlanc; P Montagna; P Cortelli; J Julien; C Vital; W W Pendelbury
Journal:  Science       Date:  1992-10-30       Impact factor: 47.728
  3 in total

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