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-Rautio, Olli Hellström, Pentti J Tienari, Tohru Matsuura, Tetsuo Ashizawa

Research output: Contribution to journalArticleScientificpeer-review

Original languageEnglish
JournalArchives of Neurology
Volume62
Pages (from-to)74-78
Number of pages5
ISSN0003-9942
Publication statusPublished - 2005
MoE publication typeA1 Journal article-refereed

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