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Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS

✍ Scribed by Janel O. Johnson; Jessica Mandrioli; Michael Benatar; Yevgeniya Abramzon; Vivianna M. Van Deerlin; John Q. Trojanowski; J. Raphael Gibbs; Maura Brunetti; Susan Gronka; Joanne Wuu; Jinhui Ding; Leo McCluskey; Maria Martinez-Lage; Dana Falcone; Dena G. Hernandez; Sampath Arepalli; Sean Chong; Jennifer C. Schymick; Jeffrey Rothstein; Francesco Landi; Yong-Dong Wang; Andrea Calvo; Gabriele Mora; Mario Sabatelli; Maria Rosaria Monsurrò; Stefania Battistini; Fabrizio Salvi; Rossella Spataro; Patrizia Sola; Giuseppe Borghero; Giuliana Galassi; Sonja W. Scholz; J. Paul Taylor; Gabriella Restagno; Adriano Chiò; Bryan J. Traynor

Book ID: 116783665
Publisher: Elsevier Science
Year: 2010
Tongue: English
Weight: 906 KB
Volume: 68
Category: Article
ISSN: 0896-6273
DOI: 10.1016/j.neuron.2010.11.036

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