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Genetic Creutzfeldt–Jakob disease with R208H mutation presenting as progressive supranuclear palsy
Author(s) -
Matěj Radoslav,
Kovacs Gabor G.,
Johanidesová Silvie,
Keller Jiří,
Matějčková Milada,
Nováková Jana,
Šigut Vladimír,
Keller Otakar,
Rusina Robert
Publication year - 2012
Publication title -
movement disorders
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.352
H-Index - 198
eISSN - 1531-8257
pISSN - 0885-3185
DOI - 10.1002/mds.24002
Subject(s) - progressive supranuclear palsy , disease , mutation , degenerative disease , medicine , neuroscience , pathology , psychology , genetics , biology , gene