 | Up a level |
Journal Article
Huebers, Annemarie, Just, Walter, Rosenbohm, Angela, Mueller, Kathrin, Marroquin, Nicolai, Goebel, Ingrid, Hoegel, Josef, Thiele, Holger, Altmueller, Janine, Nuernberg, Peter, Weishaupt, Jochen H., Kubisch, Christian 
ORCID: 0000-0003-4220-0978, Ludolph, Albert C. and Volk, Alexander E.
(2015).
De novo FUS mutations are the most frequent genetic cause in early-onset German ALS patients.
Neurobiol. Aging, 36 (11).
NEW YORK:
ELSEVIER SCIENCE INC.
ISSN 1558-1497
Naumann, Marcel, Peikert, Kevin, Guenther, Rene, van der Kooi, Anneke J., Aronica, Eleonora ORCID: 0000-0002-3542-3770, Huebers, Annemarie, Danel, Veronique, Corcia, Philippe, Pan-Montojo, Francisco, Cirak, Sebahattin, Haliloglu, Goeknur, Ludolph, Albert C., Goswami, Anand, Andersen, Peter M., Prudlo, Johannes, Wegner, Florian, Van Damme, Philip, Weishaupt, Jochen H. and Hermann, Andreas
.
Phenotypes and malignancy risk of different FUS mutations in genetic amyotrophic lateral sclerosis.
Ann. Clin. Transl. Neurol..
HOBOKEN:
WILEY.
ISSN 2328-9503