Helenius J Schelhaas
The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder
Shaw C, Shaw P, Robberecht W, Van Damme P, Veldink J, Van den Berg L, Ticozzi N, Taroni F, Gellera C, Silani V, Kirby J, Pall H, Morrison K, Al-Chalabi A, Weale M, Brown R, Landers J, Andersen P, Baas F, Vianney de Jong J, de Belleroche J, Morris A, Asbroek A, Schelhaas H, Scott K, Troakes C, Lee Y, Miller J, Johnson L, Topp S, Vance C, Shatunov A, Newhouse S, Jones A, Gray I, Wright J, Nestor P, Weber M, Sapp P, Lovestone S, Lupton M, Powell J, Rogelj B, Al-Sarraj S, Hortobágyi T, Smith B. The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder. Eur J Hum Genet 2012; 21:102-8.
Jun 13, 2012The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder
Jun 13, 2012Eur J Hum Genet 2012; 21:102-8
Shaw Christopher E, Shaw Pamela J, Robberecht Wim, Van Damme Phillip, Veldink Jan, Van den Berg Leonard, Ticozzi Nicola, Taroni Franco, Gellera Cinzia, Silani Vincenzo, Kirby Janine, Pall Hardev, Morrison Karen E, Al-Chalabi Ammar, Weale Michael E, Brown Robert H, Landers John, Andersen Peter M, Baas Frank, Vianney de Jong J M B, de Belleroche Jacqueline, Morris Alex, Asbroek Anneloor Alm Ten, Schelhaas Helenius J, Scott Kirsten M, Troakes Claire, Lee Younbok, Miller Jack, Johnson Lauren, Topp Simon, Vance Caroline, Shatunov Aleksey, Newhouse Stephen, Jones Ashley, Gray Ian, Wright Jamie, Nestor Peter J, Weber Markus, Sapp Peter C, Lovestone Simon, Lupton Michelle, Powell John, Rogelj Boris, Al-Sarraj Safa, Hortobágyi Tibor, Smith Bradley N
Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis
van den Berg L, Heutink P, van Hilten J, Verbaan D, de Visser M, van der Kooi A, Weber M, Klein C, Waibel S, Fernández-Santiago R, Birve A, Dahlberg C, Lemmens R, Hennekam E, Cuppen E, van de Warrenburg B, Landers J, de Bakker P, Pasterkamp R, Veldink J, Ophoff R, Robberecht W, Ludolph A, Gasser T, Silani V, Brown R, Berg D, Van Damme P, Pezzoli G, Keagle P, LeClerc A, Fumoto K, Diekstra F, Koppers M, Blauw H, Schulte C, Groen E, Andersen P, Ticozzi N, van Vught P, Schelhaas H, Bloem B, Scheffer H, Goldwurm S, Mariani C, Folkerth R, Wu D, Kishikawa H, Yu W, Hu G, Lowe P, Wills A, van Rheenen W, van Blitterswijk M, van Nuenen B, van Es M. Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis. Ann Neurol 2011; 70:964-73.
Dec 1, 2011Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis
Dec 1, 2011Ann Neurol 2011; 70:964-73
van den Berg Leonard H, Heutink Peter, van Hilten Jacobus J, Verbaan Dagmar, de Visser Marianne, van der Kooi Anneke J, Weber Markus, Klein Christine, Waibel Stefan, Fernández-Santiago Rubén, Birve Anna, Dahlberg Caroline, Lemmens Robin, Hennekam Eric A M, Cuppen Edwin, van de Warrenburg Bart P, Landers John E, de Bakker Paul I W, Pasterkamp R Jeroen, Veldink Jan H, Ophoff Roel A, Robberecht Wim, Ludolph Albert C, Gasser Thomas, Silani Vincenzo, Brown Robert H, Berg Daniela, Van Damme Philip, Pezzoli Gianni, Keagle Pamela, LeClerc Ashley Lyn, Fumoto Katsumi, Diekstra Frank P, Koppers Max, Blauw Hylke M, Schulte Claudia, Groen Ewout J N, Andersen Peter M, Ticozzi Nicola, van Vught Paul W J, Schelhaas Helenius J, Bloem Bastiaan R, Scheffer Hans, Goldwurm Stefano, Mariani Claudio, Folkerth Rebecca D, Wu David, Kishikawa Hiroko, Yu Wenhao, Hu Guo-fu, Lowe Patrick P, Wills Anne-Marie, van Rheenen Wouter, van Blitterswijk Marka, van Nuenen Bart F L, van Es Michael A