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Commentary for “Genetic Creutzfeldt–Jakob disease with R208H mutation presenting as progressive supranuclear palsy”
Author(s) -
Kumar Kishore R.,
Klein Christine
Publication year - 2014
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.25089
Subject(s) - neurogenetics , neurology , progressive supranuclear palsy , medicine , family medicine , psychiatry , disease , pathology