Human Genome Epidemiology Literature Finder
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Records 1 - 3 (of 3 Records) |
| Query Trace: Syndrome and KIF5A[original query] |
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| ALS and CHARGE syndrome: a clinical and genetic study. Acta neurologica Belgica 2018 10 118 (4): 629-635. Ungaro Carmine, Citrigno Luigi, Trojsi Francesca, Sprovieri Teresa, Gentile Giulia, Muglia Maria, Monsurrò Maria Rosaria, Tedeschi Gioacchino, Cavallaro Sebastiano, Conforti Francesca Lui |
| Hot-spot KIF5A mutations cause familial ALS. Brain : a journal of neurology 2018 1 141 (3): 688-697. Brenner David, Yilmaz Rüstem, Müller Kathrin, Grehl Torsten, Petri Susanne, Meyer Thomas, Grosskreutz Julian, Weydt Patrick, Ruf Wolfgang, Neuwirth Christoph, Weber Markus, Pinto Susana, Claeys Kristl G, Schrank Berthold, Jordan Berit, Knehr Antje, Günther Kornelia, Hübers Annemarie, Zeller Daniel, Kubisch Christian, Jablonka Sibylle, Sendtner Michael, Klopstock Thomas, de Carvalho Mamede, Sperfeld Anne, Borck Guntram, Volk Alexander E, Dorst Johannes, Weis Joachim, Otto Markus, 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, |
| KIF5A and the contribution of susceptibility genotypes as a predictive biomarker for multiple sclerosis. Journal of neurology 2021 Jan . Hares Kelly, Kemp K, Loveless S, Rice C M, Scolding N, Tallantyre E, Robertson N, Wilkins |
- Page last reviewed:Feb 1, 2024
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