Mutations in HTRA2 are not a common cause of familial classic ET

Mov Disord. 2015 Jul;30(8):1149-50. doi: 10.1002/mds.26252. Epub 2015 May 13.

Authors

Franziska Hopfner¹, Stefanie H Müller¹, Delia Lorenz¹, Silke Appenzeller², Stephan Klebe³, Günther Deuschl¹, Gregor Kuhlenbäumer¹

Affiliations

¹ Department of Neurology, University Hospital Schleswig Holstein, Kiel, Germany.
² Core Unit Systems Medicine, University of Würzburg, Germany.
³ Department of Neurology, University Hospital of Würzburg, Germany.

PMID: 25970799
DOI: 10.1002/mds.26252

No abstract available

Publication types

Letter

MeSH terms

Age of Onset
Aged
Disease Progression
Essential Tremor / genetics*
Female
Germany
High-Temperature Requirement A Serine Peptidase 2
Humans
Male
Middle Aged
Mitochondrial Proteins / genetics*
Mutation
Parkinson Disease / genetics
Polymorphism, Single Nucleotide
Serine Endopeptidases / genetics*

Substances

Mitochondrial Proteins
Serine Endopeptidases
HTRA2 protein, human
High-Temperature Requirement A Serine Peptidase 2