Premium
Mutations in HTRA2 are not a common cause of familial classic ET
Author(s) -
Hopfner Franziska,
Müller Stefanie H.,
Lorenz Delia,
Appenzeller Silke,
Klebe Stephan,
Deuschl Günther,
Kuhlenbäumer Gregor
Publication year - 2015
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.26252
Subject(s) - university hospital , general hospital , neurology , medicine , family medicine , psychiatry