Publications
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Filters: Author is Akiyama, Haruhiko [Clear All Filters]
“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.
