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

Cite this

Buervenich, S., Carmine, A., Galter, D., Shahabi, H. N., Johnels, B., Holmberg, B., ... Ashizawa, T. (2005). A rare truncating mutation in ADH1C (G78Stop) shows significant association with Parkinson disease in a large international sample. Archives of Neurology, 62, 74-78.
Buervenich, Silvia ; Carmine, Andrea ; Galter, Dagmar ; Shahabi, Haydeh N ; Johnels, Bo ; Holmberg, Björn ; Ahlberg, Jarl ; Nissbrandt, Hans ; Eerola-Rautio, Johanna ; Hellström, Olli ; Tienari, Pentti J ; Matsuura, Tohru ; Ashizawa, Tetsuo. / A rare truncating mutation in ADH1C (G78Stop) shows significant association with Parkinson disease in a large international sample. In: Archives of Neurology. 2005 ; Vol. 62. pp. 74-78.
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title = "A rare truncating mutation in ADH1C (G78Stop) shows significant association with Parkinson disease in a large international sample",
author = "Silvia Buervenich and Andrea Carmine and Dagmar Galter and Shahabi, {Haydeh N} and Bo Johnels and Bj{\"o}rn Holmberg and Jarl Ahlberg and Hans Nissbrandt and Johanna Eerola-Rautio and Olli Hellstr{\"o}m and Tienari, {Pentti J} and Tohru Matsuura and Tetsuo Ashizawa",
year = "2005",
language = "English",
volume = "62",
pages = "74--78",
journal = "Archives of Neurology",
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Buervenich, S, Carmine, A, Galter, D, Shahabi, HN, Johnels, B, Holmberg, B, Ahlberg, J, Nissbrandt, H, Eerola-Rautio, J, Hellström, O, Tienari, PJ, Matsuura, T & Ashizawa, T 2005, 'A rare truncating mutation in ADH1C (G78Stop) shows significant association with Parkinson disease in a large international sample' Archives of Neurology, vol. 62, pp. 74-78.

A rare truncating mutation in ADH1C (G78Stop) shows significant association with Parkinson disease in a large international sample. / Buervenich, Silvia; Carmine, Andrea; Galter, Dagmar; Shahabi, Haydeh N; Johnels, Bo; Holmberg, Björn; Ahlberg, Jarl; Nissbrandt, Hans; Eerola-Rautio, Johanna; Hellström, Olli; Tienari, Pentti J; Matsuura, Tohru; Ashizawa, Tetsuo.

In: Archives of Neurology, Vol. 62, 2005, p. 74-78.

Research output: Contribution to journalArticleScientificpeer-review

TY - JOUR

T1 - A rare truncating mutation in ADH1C (G78Stop) shows significant association with Parkinson disease in a large international sample

AU - Buervenich, Silvia

AU - Carmine, Andrea

AU - Galter, Dagmar

AU - Shahabi, Haydeh N

AU - Johnels, Bo

AU - Holmberg, Björn

AU - Ahlberg, Jarl

AU - Nissbrandt, Hans

AU - Eerola-Rautio, Johanna

AU - Hellström, Olli

AU - Tienari, Pentti J

AU - Matsuura, Tohru

AU - Ashizawa, Tetsuo

PY - 2005

Y1 - 2005

M3 - Article

VL - 62

SP - 74

EP - 78

JO - Archives of Neurology

JF - Archives of Neurology

SN - 0003-9942

ER -