Cases, Statutes and Recent Developments von Dowell, Diana, Helt, Michael, Warhurst, Martin, Caldwell, Jim, Bredesen, Karsten, Trosen, Wallace, Impey, Jim, Cone, Pamela, Schaeffer, Jeanne, Allen, Harvey, Dudley, Christina, Mahan, Hurley D., Muren, Terri, Arras, Tom, Lamkin, Marcia, Francis, Connie, Miller, Lee Ann, Fluker, James, Nichols, Brenda L., Harmison, Cynthia, Stipp, Lori, Holton, Ellen P., Ground, Deborah, Poskin, David, Gall, Joe, Marske, Larry K., Greenhagen, Russell, Entwistle, Barbara, Robinson, Laurie

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Cryptic Amyloidogenic Elements in the 3′ UTRs of Neurofilament Genes Trigger Axonal Neuropathy von Rebelo, Adriana P., Abrams, Alexander J., Cottenie, Ellen, Horga, Alejandro, Gonzalez, Michael, Bis, Dana M., Sanchez-Mejias, Avencia, Pinto, Milena, Buglo, Elena, Markel, Kasey, Prince, Jeffrey, Laura, Matilde, Houlden, Henry, Blake, Julian, Woodward, Cathy, Sweeney, Mary G., Holton, Janice L., Hanna, Michael, Dallman, Julia E., Auer-Grumbach, Michaela, Reilly, Mary M., Zuchner, Stephan

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Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study von Jabbari, Edwin, Koga, Shunsuke, Valentino, Rebecca R, Reynolds, Regina H, Ferrari, Raffaele, Tan, Manuela M X, Rowe, James B, Dalgard, Clifton L, Scholz, Sonja W, Dickson, Dennis W, Warner, Thomas T, Revesz, Tamas, Höglinger, Günter U, Ross, Owen A, Ryten, Mina, Hardy, John, Shoai, Maryam, Morris, Huw R, Mok, Kin Y., Murphy, David P., Al-Sarraj, Safa, Troakes, Claire, Gentleman, Steve M., Allinson, Kieren S.J., Jaunmuktane, Zane, Holton, Janice L., Lees, Andrew J., Morris, Christopher M., Compta, Yaroslau, Gelpi, Ellen, van Swieten, John C., Rajput, Alex, Ferguson, Leslie, Cookson, Mark R., Gibbs, J. Raphael, Blauwendraat, Cornelis, Ding, Jinhui, Chia, Ruth, Traynor, Bryan J., Pantelyat, Alexander, Viollet, Coralie, Pletnikova, Olga, Troncoso, Juan C., Rosenthal, Liana S., Boxer, Adam L., Respondek, Gesine, Arzberger, Thomas, Roeber, Sigrun, Giese, Armin, Burn, David J., Pavese, Nicola, Gerhard, Alexander, Kobylecki, Christopher, Leigh, P. Nigel, Church, Alistair, T.M. Hu, Michele

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Genetic dysfunction of MT-ATP6 causes axonal Charcot-Marie-Tooth disease von Pitceathly, Robert D S, Murphy, Sinéad M, Cottenie, Ellen, Chalasani, Annapurna, Sweeney, Mary G, Woodward, Cathy, Mudanohwo, Ese E, Hargreaves, Iain, Heales, Simon, Land, John, Holton, Janice L, Houlden, Henry, Blake, Julian, Champion, Michael, Flinter, Frances, Robb, Stephanie A, Page, Rupert, Rose, Michael, Palace, Jacqueline, Crowe, Carol, Longman, Cheryl, Lunn, Michael P, Rahman, Shamima, Reilly, Mary M, Hanna, Michael G

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Genetic dysfunction of MT-A TP6 causes axonal Charcot-Marie-Tooth disease von PITCEATHLY, Robert D. S, MURPHY, Sinéad M, HOLTON, Janice L, HOULDEN, Henry, BLAKE, Julian, CHAMPION, Michael, FLINTER, Frances, ROBB, Stephanie A, PAGE, Rupert, ROSE, Michael, PALACE, Jacqueline, CROWE, Carol, COTTENIE, Ellen, LONGMAN, Cheryl, LUNN, Michael P, RAHMAN, Shamima, REILLY, Mary M, HANNA, Michael G, CHALASANI, Annapurna, SWEENEY, Mary G, WOODWARD, Cathy, MUDANOHWO, Ese E, HARGREAVES, Iain, HEALES, Simon, LAND, John

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