Slow disease progression and characteristic TDP-43 inclusions in a patient with familial amyotrophic lateral sclerosis carrying a TARDBP G357S variant.
Makoto SainouchiShinya OginezawaMari TadaTomohiko IshiharaOsamu OnoderaAkiyoshi KakitaPublished in: Neuropathology and applied neurobiology (2024)