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A postzygotic de novo NCDN mutation identified in a sporadi..:
Nicolas, Gaël
;
Sévigny, Myriam
;
Lecoquierre, François
...
Acta Neuropathologica Communications. 10 (2022) 1 - p. , 2022
Link:
https://doi.org/10.1186/s40478-022-01314-x
RT Journal T1
A postzygotic de novo NCDN mutation identified in a sporadic FTLD patient results in neurochondrin haploinsufficiency and altered FUS granule dynamics
UL https://suche.suub.uni-bremen.de/peid=cr-10.1186_s40478-022-01314-x&Exemplar=1&LAN=DE A1 Nicolas, Gaël A1 Sévigny, Myriam A1 Lecoquierre, François A1 Marguet, Florent A1 Deschênes, Andréanne A1 del Pelaez, Maria Carment A1 Feuillette, Sébastien A1 Audebrand, Anaïs A1 Lecourtois, Magalie A1 Rousseau, Stéphane A1 Richard, Anne-Claire A1 Cassinari, Kévin A1 Deramecourt, Vincent A1 Duyckaerts, Charles A1 Boland, Anne A1 Deleuze, Jean-François A1 Meyer, Vincent A1 Clarimon Echavarria, Jordi A1 Gelpi, Ellen A1 Akiyama, Haruhiko A1 Hasegawa, Masato A1 Kawakami, Ito A1 Wong, Tsz H. A1 Van Rooij, Jeroen G. J. A1 Van Swieten, John C. A1 Campion, Dominique A1 Dutchak, Paul A. A1 Wallon, David A1 Lavoie-Cardinal, Flavie A1 Laquerrière, Annie PB Springer Science and Business Media LLC YR 2022 SN 2051-5960 JF Acta Neuropathologica Communications VO 10 IS 1 LK http://dx.doi.org/https://doi.org/10.1186/s40478-022-01314-x DO https://doi.org/10.1186/s40478-022-01314-x SF ELIB - SuUB Bremen
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