-
1
المؤلفون: Kenna, K.P., van Doormaal, P.T.C., Dekker, A.M., Ticozzi, N., Kenna, B.J., Diekstra, F.P., van Rheenen, W., van Eijk, K.R., Jones, A.R., Keagle, P., Shatunov, A., Sproviero, W., Smith, B.N., van Es, M.A., Topp, S.D., Kenna, A., Miller, J.W., Fallini, C., Tiloca, C., McLaughlin, R.L., Vance, C., Troakes, C., Colombrita, C., Mora, G., Calvo, A., Verde, F., Al-Sarraj, S., King, A., Calini, D., de Belleroche, J., Baas, F., van der Kooi, A.J., de Visser, M., ten Asbroek, A.L.M.A., Sapp, P.C., McKenna-Yasek, D., Polak, M., Asress, S., Muñoz-Blanco, J.L., Strom, T.M., Meitinger, T., Morrison, K.E., D'Alfonso, S., Mazzini, L., Comi, G.P., Del Bo, R., Ceroni, M., Gagliardi, S., Querin, G., Bertolin, C., Pensato, V., Castellotti, B., Corti, S., Cereda, C., Corrado, L., Sorarù, G., Lauria, G., Williams, K.L., Leigh, P.N., Nicholson, G.A., Blair, I.P., Leblond, C.S., Dion, P.A., Rouleau, G.A., Pall, H., Shaw, P.J., Turner, M.R., Talbot, K., Taroni, F., Boylan, K.B., Van Blitterswijk, M., Rademakers, R., Esteban-Pérez, J., García-Redondo, A., Van Damme, P., Robberecht, W., Chio, A., Gellera, C., Drepper, C., Sendtner, M., Ratti, A., Glass, J.D., Mora, J.S., Basak, N.A., Hardiman, O., Ludolph, A.C., Andersen, P.M., Weishaupt, J.H., Brown, R.H., Al-Chalabi, A., Silani, V., Shaw, C.E., van den Berg, L.H., Veldink, J.H., Landers, J.E.
المساهمون: Medical Research Council (MRC), Human Genetics, Neurology, ANS - Neurodegeneration, SLAGEN Consortium
المصدر: Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Nature genetics, 48(9), 1037-1042. Nature Publishing Group
Nature Genetics, 48(9), 1037–1042. Nature Publishing Group
Nature geneticsمصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, Genomics, Biology, medicine.disease_cause, Article, Cohort Studies, 03 medical and health sciences, 0302 clinical medicine, Journal Article, Genetics, medicine, Humans, Comparative Study, Exome, Genetic Predisposition to Disease, SLAGEN Consortium, Risk factor, Amyotrophic lateral sclerosis, Gene, Genetic Association Studies, Netherlands, Mutation, Amyotrophic Lateral Sclerosis, Case-control study, 11 Medical And Health Sciences, 06 Biological Sciences, medicine.disease, 3. Good health, NIMA-Related Kinase 1, 030104 developmental biology, RC0346, Case-Control Studies, Medical genetics, Human medicine, 030217 neurology & neurosurgery, Developmental Biology
وصف الملف: application/pdf; text; image/pdf; Print-Electronic
-
2Academic Journal
المؤلفون: Nicolas, A., Kenna, K.P., Renton, A.E., Ticozzi, N., Faghri, F., Chia, R., Dominov, J.A., Kenna, B.J., Nalls, M.A., Keagle, P., Rivera, A.M., van Rheenen, W., Murphy, N.A., van Vugt, J.J.F.A., Geiger, J.T., van der Spek, R.A., Pliner, H.A., Shankaracharya, B.N.S., Smith, B.N., Marangi, G., Topp, S.D., Abramzon, Y., Gkazi, A.S., Eicher, J.D., Kenna, A., Mora, G., Calvo, A., Mazzini, L., Riva, N., Mandrioli, J., Caponnetto, C., Battistini, S., Volanti, P., La Bella, V., Conforti, F.L., Borghero, G., Messina, S., Simone, I.L., Trojsi, F., Salvi, F., Logullo, F.O., D'Alfonso, S., Corrado, L., Capasso, M., Ferrucci, L., Moreno, C.A.M., Kamalakaran, S., Goldstein, D.B., Gitler, A.D., Harris, T., Myers, R.M., Phatnani, H., Musunuri, R.L., Evani, U.S., Abhyankar, A., Zody, M.C., Kaye, J., Finkbeiner, S., Wyman, S.K., LeNail, A., Lima, L., Fraenkel, E., Svendsen, C.N., Thompson, L.M., Van Eyk, J.E., Berry, J.D., Miller, T.M., Kolb, S.J., Cudkowicz, M., Baxi, E., Benatar, M., Taylor, J.P., Rampersaud, E., Wu, G.M., Wuu, J., Lauria, G., Verde, F., Fogh, I., Tiloca, C., Comi, G.P., Sorarù, G., Cereda, C., Corcia, P., Laaksovirta, H., Myllykangas, L., Jansson, L., Valori, M., Ealing, J., Hamdalla, H., Rollinson, S., Pickering-Brown, S., Orrell, R.W., Sidle, K.C., Malaspina, A., Hardy, J., Singleton, A.B., Johnson, J.O., Arepalli, S., Sapp, P.C., McKenna-Yasek, D., Polak, M., Asress, S., Al-Sarraj, S., King, A., Troakes, C., Vance, C., de Belleroche, J., Baas, F., Ten Asbroek, A.L.M.A., Muñoz-Blanco, J.L., Hernandez, D.G., Ding, J., Gibbs, J.R., Scholz, S.W., Floeter, M.K., Campbell, R.H., Landi, F., Bowser, R., Pulst, S.M., Ravits, J.M., MacGowan, D.J.L., Kirby, J., Pioro, E.P., Pamphlett, R., Broach, J., Gerhard, G., Dunckley, T.L., Brady, C.B., Kowall, N.W., Troncoso, J.C., Le Ber, I., Mouzat, K., Lumbroso, S., Heiman-Patterson, T.D., Kamel, F., Van Den Bosch, L., Baloh, R.H., Strom, T.M., Meitinger, T., Shatunov, A., van Eijk, K.R., de Carvalho, M., Kooyman, M., Middelkoop, B., Moisse, M., McLaughlin, R.L., van Es, M.A., Weber, M., Boylan, K.B., van Blitterswijk, M., Rademakers, R., Morrison, K.E., Basak, A.N., Mora, J.S., Drory, V.E., Shaw, P.J., Turner, M.R., Talbot, K., Hardiman, O., Williams, K.L., Fifita, J.A., Nicholson, G.A., Blair, I.P., Rouleau, G.A., Esteban-Pérez, J., García-Redondo, A., Al-Chalabi, A., Rogaeva, E., Zinman, L., Ostrow, L.W., Maragakis, N.J., Rothstein, J.D., Simmons, Z., Cooper-Knock, J., Brice, A., Goutman, S.A., Feldman, E.L., Gibson, S.B., Taroni, F., Ratti, A., Gellera, C., van Damme, P., Robberecht, W., Fratta, P., Sabatelli, M., Lunetta, C., Ludolph, A.C., Andersen, P.M., Weishaupt, J.H., Camu, W., Trojanowski, J.Q., van Deerlin, V.M., Brown, R.H., van den Berg, L.H., Veldink, J.H., Harms, M.B., Glass, J.D., Stone, D.J., Tienari, P., Silani, V., Chio, A., Shaw, C.E., Traynor, B.J., Landers, J.E.
المصدر: Neuron 97, 1268-1283.e6 (2018)
Relation: info:eu-repo/semantics/altIdentifier/pmid/29566793; info:eu-repo/semantics/altIdentifier/wos/WOS:000428235400013; info:eu-repo/semantics/altIdentifier/isbn/0896-6273; info:eu-repo/semanti