Bigio, E. H., Wu, J. Y., Deng, H., Bit-Ivan, E. N., Mao, Q., Ganti, R., . . . Mesulam, M. (2013). Inclusions in frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP) and amyotrophic lateral sclerosis (ALS), but not FTLD with FUS proteinopathy (FTLD-FUS), have properties of amyloid.
Chicago-стиль цитированияBigio, Eileen H., et al. Inclusions in Frontotemporal Lobar Degeneration With TDP-43 Proteinopathy (FTLD-TDP) and Amyotrophic Lateral Sclerosis (ALS), but Not FTLD With FUS Proteinopathy (FTLD-FUS), Have Properties of Amyloid. 2013.
MLA-цитированиеBigio, Eileen H., et al. Inclusions in Frontotemporal Lobar Degeneration With TDP-43 Proteinopathy (FTLD-TDP) and Amyotrophic Lateral Sclerosis (ALS), but Not FTLD With FUS Proteinopathy (FTLD-FUS), Have Properties of Amyloid. 2013.