Phenotypic variability in a large kindred (Family LA) with deletions in the parkin gene

Peter P. Pramstaller, Bernhard Kis, Cordula Eskelson, Katja Hedrich, Monika Scherer, Eberhard Schwinger, Xandra O. Breakefield, Patricia L. Kramer, Laurie J. Ozelius, Christine Klein

Research output: Contribution to journalArticle

20 Scopus citations
Original languageEnglish (US)
Pages (from-to)424-426
Number of pages3
JournalMovement Disorders
Volume17
Issue number2
DOIs
StatePublished - Mar 2002

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

Cite this

Pramstaller, P. P., Kis, B., Eskelson, C., Hedrich, K., Scherer, M., Schwinger, E., Breakefield, X. O., Kramer, P. L., Ozelius, L. J., & Klein, C. (2002). Phenotypic variability in a large kindred (Family LA) with deletions in the parkin gene. Movement Disorders, 17(2), 424-426. https://doi.org/10.1002/mds.10071