Publications
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Filtres: Author is Akiyama, Haruhiko [Enlever les filtres]
, « A postzygotic de novo NCDN mutation identified in a sporadic FTLD patient results in neurochondrin haploinsufficiency and altered FUS granule dynamics. », Acta Neuropathol Commun, vol. 10, nᵒ 1, p. 20, 2022.
, « The Src/c-Abl pathway is a potential therapeutic target in amyotrophic lateral sclerosis. », Sci Transl Med, vol. 9, nᵒ 391, 2017.
