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Publicações a aguardarem confirmação

1
TITLE: Correction: Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment (Genetics in Medicine, (2020), 22, 11, (1851-1862), 10.1038/s41436-020-0899-x)
AUTHORS: Roux, T; Barbier, M; Papin, M; Davoine, CS; Sayah, S; Coarelli, G; Charles, P; Marelli, C; Parodi, L; Tranchant, C; Goizet, C; Klebe, S; Lohmann, E; Van Maldergem, L; van Broeckhoven, C; Coutelier, M; Tesson, C; Stevanin, G; Duyckaerts, C; Brice, A; Durr, A; Durr, A; Stevanin, G; Brice, A; Darios, F; Forlani, S; Site, PS; Banneau, G; Cazeneuve, C; Charles, P; Duyckaerts, C; Fontaine, B; Azulay, JP; Boesfplug Tanguy, O; Goizet, C; Hannequin, D; Hazan, J; Burgo, A; Verny, C; Koenig, M; Labauge, P; Marelli, C; N’guyen, K; Rodriguez, D; Belarbi, S; Hamri, A; Tazir, M; Boesch, S; Pandolfo, M; Laura, J; Guergueltcheva, V; Tournev, I; Pedraza Linarès, OL; Nielsen, JE; Svenstrup, K; Zaki, M; Bauer, P; Schöls, L; Schüle, R; Lossos, A; Bassi, MT; Basso, M; Bertini, E; Brusco, A; Casali, C; Casari, G; Criscuolo, C; Filla, A; Orsi, L; Santorelli, FM; Valente, EM; Vavla, M; Vazza, G; Megarbane, A; Benomar, A; Kremer, B; Van Roon Mom, W; Roxburgh, R; Erichsen, AK; Tallaksen, C; Alonso, I; Coutinho, P; Loureiro, JL; Sequeiros, J; Salih, M; Kostic, VS; Rouco Axpe, I; Elsayed, L; Paucar, MA; Roumani, S; Bing Wen, S; Reid, E; Suran, N; Warner, T; Wood, N; ...More
PUBLISHED: 2020, SOURCE: Genetics in Medicine
INDEXED IN: Scopus

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