z-logo
Premium
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

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom