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pro vyhledávání: '"Sendtner, Michael"'
Autor:
Brenner, David, Yilmaz, Rüstem, Weber, Markus, Pinto, Susana, Claeys, Kristl, Schrank, Berthold, Jordan, Berit, Knehr, Antje, Günther, Kornelia, Hübers, Annemarie, Zeller, Daniel, Kubisch, Christian, Müller, Kathrin, Jablonka, Sibylle, Sendtner, Michael, Klopstock, Thomas, de Carvalho, Mamede, Sperfeld, Anne, Borck, Guntram, Volk, Alexander E., Dorst, Johannes, Weis, Joachim, Otto, Markus, Grehl, Torsten, Schuster, Joachim, Del Tredici, Kelly, Braak, Heiko, Danzer, Karin M., Freischmidt, Axel, Meitinger, Thomas, Strom, Tim M., Ludolph, Albert C., Andersen, Peter M., Weishaupt, Jochen H., Petri, Susanne, German ALS network MND-NET, Weyen, Ute, Hermann, Andreas, Hagenacker, Tim, Koch, Jan Christoph, Lingor, Paul, Göricke, Bettina, Zierz, Stephan, Baum, Petra, Wolf, Joachim, Meyer, Thomas, Winkler, Andrea, Young, Peter, Bogdahn, Ulrich, Prudlo, Johannes, Kassubek, Jan, Grosskreutz, Julian, Weydt, Patrick, Ruf, Wolfgang, Neuwirth, Christoph
Publikováno v:
Brain : a journal of neurology 141(3), 688-697 (2018). doi:10.1093/brain/awx370
Brain
PubMed Central
Publikationer från Umeå universitet
OpenAIRE
Lirias
Brain 141(3), 688-697 (2018). doi:10.1093/brain/awx370
Brain
PubMed Central
Publikationer från Umeå universitet
OpenAIRE
Lirias
Brain 141(3), 688-697 (2018). doi:10.1093/brain/awx370
Brenner et al. show that mutations in a C-terminal hotspot of kinesin-5A (KIF5A) can cause a classical ALS phenotype. Experiments using patient-derived cell lines suggest haploinsufficiency as the molecular genetic mechanism. This underlines the rele
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c3f40d2dcee1873508c7948349c21d0
https://lirias.kuleuven.be/handle/123456789/611026
https://lirias.kuleuven.be/handle/123456789/611026