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

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

*Corresponding author for this work
Original languageEnglish
JournalJournal of Neurology
Volume261
Issue number4
Pages (from-to)833-834
Number of pages2
ISSN0340-5354
DOIs
Publication statusPublished - 01.01.2014

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being
  2. SDG 10 - Reduced Inequalities
    SDG 10 Reduced Inequalities

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