Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS-Reference-Cited by-同舟云学术

Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS

Published:2010-12 Issue:5 Volume:68 Page:857-864
ISSN:0896-6273
Container-title:Neuron
language:en
Short-container-title:Neuron

Author:

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

Publisher

Elsevier BV

Subject

General Neuroscience

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