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Probable genetic Creutzfeldt-Jakob Disease with rare E196K mutation.
Orlewska K, Błońska M, Błoński Ł, Madej Ł, Klusek J. Orlewska K, et al. Among authors: blonski l. Neurol Neurochir Pol. 2021;55(1):113-114. doi: 10.5603/PJNNS.a2021.0009. Epub 2021 Feb 2. Neurol Neurochir Pol. 2021. PMID: 33528834 Free article. No abstract available.