AlaSOPro mutation in the gene encoding α-synuclein in Parkinson's disease (original) (raw)
- Correspondence
- Published: 01 February 1998
- Wilfried Kuhn1,
- Thomas Müller1,
- Dirk Woitalla1,
- Manuel Graeber3,4,
- Sigfried Kösel1,
- Horst Przuntek1,
- Jörg T. Epplen2,
- Ludger Schols1 &
- …
- Olaf Riess2,1
Nature Genetics volume 18, pages 106–108 (1998)Cite this article
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Authors and Affiliations
- Neurological University Hospital, Ruhr-University, 44780, Bochum, Germany
Rejko Krüger, Wilfried Kuhn, Thomas Müller, Dirk Woitalla, Sigfried Kösel, Horst Przuntek, Ludger Schols & Olaf Riess - Department of Molecular Human Genetics, Ruhr-University, 44780, Bochum, Germany
Rejko Krüger, Jörg T. Epplen & Olaf Riess - Department of Neuromorphology, Max-Planck-Institute for Psychiatry, 82152, Martinsried, Germany
Manuel Graeber - Institute of Molecular Neuropathology, 80337, Munich, Germany
Manuel Graeber
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Krüger, R., Kuhn, W., Müller, T. et al. AlaSOPro mutation in the gene encoding α-synuclein in Parkinson's disease.Nat Genet 18, 106–108 (1998). https://doi.org/10.1038/ng0298-106
- Issue Date: 01 February 1998
- DOI: https://doi.org/10.1038/ng0298-106