Probable genetic Creutzfeldt-Jakob Disease with rare E196K mutation
Neurol Neurochir Pol
.
2021;55(1):113-114.
doi: 10.5603/PJNNS.a2021.0009.
Epub 2021 Feb 2.
Authors
Katarzyna Orlewska
1
,
Monika Błońska
2
,
Łukasz Błoński
2
,
Łukasz Madej
3
,
Justyna Klusek
3
Affiliations
1
Tytus Chałubiński's Hospital, Zakopane, Poland. korlewska@gmail.com.
2
Tytus Chałubiński's Hospital, Zakopane, Poland.
3
Collegium Medicum, Jan Kochanowski University, Kielce, Poland.
PMID:
33528834
DOI:
10.5603/PJNNS.a2021.0009
No abstract available
Keywords:
E196K mutation; genetic Creutzfeldt-Jakob Disease.
Publication types
Research Support, Non-U.S. Gov't
MeSH terms
Creutzfeldt-Jakob Syndrome* / genetics
Humans
Mutation