The recurrent mutation Arg258Gln in SYNJ1 (PARK20) is not a common cause of Parkinson's disease

J Neurol. 2014 Apr;261(4):833-4. doi: 10.1007/s00415-014-7306-y. Epub 2014 Mar 9.

Authors

Susen Winkler¹, Eva-Juliane Vollstedt, Meike Kasten, Daniel Alvarez-Fischer, Christine Klein, Katja Lohmann

Affiliation

¹ Institute of Neurogenetics, University of Lübeck, Ratzeburger Allee 160, 23538, Lübeck, Germany.

PMID: 24609975
DOI: 10.1007/s00415-014-7306-y

No abstract available

Publication types

Letter
Research Support, Non-U.S. Gov't

MeSH terms

Adolescent
Adult
Aged
Aged, 80 and over
Child
Female
Humans
Male
Middle Aged
Mutation / genetics
Mutation / physiology
Parkinson Disease / etiology
Parkinson Disease / genetics*
Phosphoric Monoester Hydrolases / genetics*
Young Adult

Substances

Phosphoric Monoester Hydrolases
phosphoinositide 5-phosphatase