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Brain Res. Mol. Brain Res. · Dec 1995
Case ReportsPrion disease associated with a novel nine octapeptide repeat insertion in the PRNP gene.
- S Krasemann, I Zerr, T Weber, S Poser, H Kretzschmar, G Hunsmann, and W Bodemer.
- Department of Virology and Immunology, German Primate Centre, Göttingen, Germany.
- Brain Res. Mol. Brain Res. 1995 Dec 1;34(1):173-6.
AbstractSome cases of spongiform encephalopathies are linked to mutations within the prion protein gene (PRNP). Repetitive octapeptide insertions of variable length in the PRNP gene are also associated with spongiform encephalopathies, mostly familial Creutzfeldt-Jakob disease (CJD). In this study we report on a novel insertion mutation comprising nine extra octapeptide repeats between codons 51 and 91 of the PRNP gene. The affected patient showed a slowly progressive dementia of at least 6 years duration and ataxia.
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