Tim M Strom
Hot-spot KIF5A mutations cause familial ALS
Weishaupt J, Weis J, Dorst J, Volk A, Borck G, Sperfeld A, de Carvalho M, Klopstock T, Sendtner M, Otto M, Schuster J, Andersen P, Ludolph A, Strom T, Meitinger T, Freischmidt A, Danzer K, Braak H, Del Tredici K, Jablonka S, Kubisch C, German ALS network MND-NET, Ruf W, Weydt P, Grosskreutz J, Meyer T, Petri S, Grehl T, Müller K, Yilmaz R, Neuwirth C, Weber M, Zeller D, Hübers A, Günther K, Knehr A, Jordan B, Schrank B, Claeys K, Pinto S, Brenner D. Hot-spot KIF5A mutations cause familial ALS. Brain 2018
Jan 12, 2018Hot-spot KIF5A mutations cause familial ALS
Jan 12, 2018Brain 2018
Weishaupt Jochen H, Weis Joachim, Dorst Johannes, Volk Alexander E, Borck Guntram, Sperfeld Anne, de Carvalho Mamede, Klopstock Thomas, Sendtner Michael, Otto Markus, Schuster Joachim, Andersen Peter M, Ludolph Albert C, Strom Tim M, Meitinger Thomas, Freischmidt Axel, Danzer Karin M, Braak Heiko, Del Tredici Kelly, Jablonka Sibylle, Kubisch Christian, German ALS network MND-NET, Ruf Wolfgang, Weydt Patrick, Grosskreutz Julian, Meyer Thomas, Petri Susanne, Grehl Torsten, Müller Kathrin, Yilmaz Rüstem, Neuwirth Christoph, Weber Markus, Zeller Daniel, Hübers Annemarie, Günther Kornelia, Knehr Antje, Jordan Berit, Schrank Berthold, Claeys Kristl G, Pinto Susana, Brenner David
NEK1 mutations in familial amyotrophic lateral sclerosis
Brenner D, Danzer K, Volk A, Meitinger T, Strom T, Otto M, Kassubek J, Ludolph A, Andersen P, Wahlqvist M, Borck G, Müller K, Wieland T, Weydt P, Böhm S, Lule D, Hübers A, Neuwirth C, Weber M, Weishaupt J. NEK1 mutations in familial amyotrophic lateral sclerosis. Brain 2016
Mar 5, 2016NEK1 mutations in familial amyotrophic lateral sclerosis
Mar 5, 2016Brain 2016
Brenner David, Danzer Karin M, Volk Alexander E, Meitinger Thomas, Strom Tim M, Otto Markus, Kassubek Jan, Ludolph Albert C, Andersen Peter M, Wahlqvist Magnus, Borck Guntram, Müller Kathrin, Wieland Thomas, Weydt Patrick, Böhm Sarah, Lule Dorotheé, Hübers Annemarie, Neuwirth Christoph, Weber Markus, Weishaupt Jochen H
Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits
Horn D, Illig T, Bezzina C, Franke A, Spranger S, Villavicencio-Lorini P, Seifert W, Rosenfeld J, Klopocki E, Rappold G, Wohlleber E, Riess O, Bonin M, Kapeller J, Rivera-Brugués N, Moog U, Lorenz-Depiereux B, Eck S, Hempel M, Wagenstaller J, Gawthrope A, Monaco A, Strom T. Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits. Hum Mutat 2010; 31:E1851-60.
Nov 1, 2010Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits
Nov 1, 2010Hum Mutat 2010; 31:E1851-60
Horn Denise, Illig Thomas, Bezzina Connie R, Franke Andre, Spranger Stephanie, Villavicencio-Lorini Pablo, Seifert Wenke, Rosenfeld Jochen, Klopocki Eva, Rappold Gudrun A, Wohlleber Eva, Riess Olaf, Bonin Michael, Kapeller Johannes, Rivera-Brugués Núria, Moog Ute, Lorenz-Depiereux Bettina, Eck Sebastian, Hempel Maja, Wagenstaller Janine, Gawthrope Alex, Monaco Anthony P, Strom Tim M