Literature DB >> 1353344

Uncommon phenotype for a codon 178 mutation of the human PrP gene.

J L Laplanche, J Chatelain, S Thomas, J M Launay, C Gaultier, C Derouesne.   

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Year:  1992        PMID： 1353344     DOI： 10.1002/ana.410310321

Source DB:  PubMed          Journal:  Ann Neurol        ISSN： 0364-5134            Impact factor:   10.422


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  2 in total

Review 1.  Prions, beta-sheets and transmissible dementias: is there still something missing?

Authors:  P P Liberski
Journal:  Acta Neuropathol       Date:  1995       Impact factor: 17.088

2.  Codon 178 mutation of the human prion protein gene in a German family (Backer family): sequencing data from 72-year-old celloidin-embedded brain tissue.

Authors:  H A Kretzschmar; M Neumann; D Stavrou
Journal:  Acta Neuropathol       Date:  1995       Impact factor: 17.088
  2 in total

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