Erratum exome sequencing reveals VCP mutations as a cause of familial ALS

Janel O. Johnson, Jessica Mandrioli, Michael G 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 LandiYong 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

Research output: Contribution to journalArticle

5 Scopus citations
Original languageEnglish
JournalNeuron
Volume69
Issue number2
DOIs
StatePublished - Jan 27 2011
Externally publishedYes

ASJC Scopus subject areas

  • Neuroscience(all)

Cite this

Johnson, J. O., Mandrioli, J., Benatar, M. G., Abramzon, Y., Van Deerlin, V. M., Trojanowski, J. Q., Gibbs, J. R., Brunetti, M., Gronka, S., Wuu, J., Ding, J., McCluskey, L., Martinez-Lage, M., Falcone, D., Hernandez, D. G., Arepalli, S., Chong, S., Schymick, J. C., Rothstein, J., ... Traynor, B. J. (2011). Erratum exome sequencing reveals VCP mutations as a cause of familial ALS. Neuron, 69(2). https://doi.org/10.1016/j.neuron.2011.01.009