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A rare truncating mutation in ADH1C (G78stop) shows significant association with Parkinson disease in a large international sample
Silvia Buervenich, Andrea Carmine, Dagmar Galter, Haydeh N. Shahabi, Bo Johnels, Björn Holmberg, Jarl Ahlberg, Hans Nissbrandt, Johanna Eerola, Olli Hellström, Pentti J. Tienari, Tohru Matsuura, Tetsuo Ashizawa, Ullrich Wüllner, Thomas Klockgether, Alexander Zimprich, Thomas Gasser, Melissa Hanson, Shamaila Waseem, Andrew Singleton
Research output: Contribution to journal › Article › peer-review
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Scopus
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