Articles with "associated g131v" as a keyword



Photo by camstejim from unsplash

An unusual familial dementia associated with G131V PRNP mutation

Sign Up to like & get
recommendations!
Published in 2020 at "European Journal of Neurology"

DOI: 10.1111/ene.14559

Abstract: Gerstmannā€Struasslerā€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