An unusual familial dementia associated with G131V PRNP mutation
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DOI: 10.1111/ene.14559
Abstract: Gerstmann‐Struassler‐Scheinker disease is one of the familial prion diseases secondary to mutations in the prion protein gene (PRNP). The clinical phenotype has a diverse spectrum and might show variation among cases with the same genotype.… read more here.
Keywords: prnp; dementia associated; unusual familial; familial dementia ... See more keywords