The role of de novo mutations in the development of amyotrophic lateral sclerosis
Doormaal, Perry T.C., Ticozzi, Nicola, Weishaupt, Jochen H., Kenna, Kevin, Diekstra, Frank P., Verde, Federico, Andersen, Peter M., Dekker, Annelot M., Tiloca, Cinzia, Marroquin, Nicolai, Overste, Daniel J., Pensato, Viviana, Nürnberg, Peter, Pulit, Sara L., Schellevis, Raymond D., Calini, Daniela, Altmüller, Janine, Francioli, Laurent C., Muller, Bernard, Castellotti, Barbara, Motameny, Susanne, Ratti, Antonia, Wolf, Joachim, Gellera, Cinzia, Ludolph, Albert C., den Berg, Leonard H., Kubisch, Christian, Landers, John E., Veldink, Jan H., Silani, Vincenzo, Volk, Alexander E.
Published in Human mutation (01.11.2017)
Published in Human mutation (01.11.2017)
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No mutations in hnRNPA1 and hnRNPA2B1 in Dutch patients with amyotrophic lateral sclerosis, frontotemporal dementia, and inclusion body myopathy
Seelen, Meinie, Visser, Anne E, Overste, Daniel J, Kim, Hong J, Palud, A, Wong, Tsz H, van Swieten, John C, Scheltens, Philip, Voermans, Nicol C, Baas, Frank, de Jong, J.M.B.V, van der Kooi, Anneke J, de Visser, Marianne, Veldink, Jan H, Taylor, J. Paul, Van Es, Michael A, van den Berg, Leonard H
Published in Neurobiology of aging (01.08.2014)
Published in Neurobiology of aging (01.08.2014)
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