A Rare Truncating Mutation in ADH1C (G78Stop) Shows Significant Association With Parkinson Disease in a Large International Sample-Reference-Cited by-同舟云学术

A Rare Truncating Mutation in ADH1C (G78Stop) Shows Significant Association With Parkinson Disease in a Large International Sample

Published:2005-01-01 Issue:1 Volume:62 Page:74
ISSN:0003-9942
Container-title:Archives of Neurology
language:en
Short-container-title:Arch Neurol

Author:

Buervenich Silvia,Carmine Andrea,Galter Dagmar,Shahabi Haydeh N.,Johnels Bo,Holmberg Björn,Ahlberg Jarl,Nissbrandt Hans,Eerola Johanna,Hellström Olli,Tienari Pentti J.,Matsuura Tohru,Ashizawa Tetsuo,Wüllner Ullrich,Klockgether Thomas,Zimprich Alexander,Gasser Thomas,Hanson Melissa,Waseem Shamaila,Singleton Andrew,McMahon Francis J.,Anvret Maria,Sydow Olof,Olson Lars

Publisher

American Medical Association (AMA)

Subject

Neurology (clinical),Arts and Humanities (miscellaneous)

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