An autopsy report of a familial amyotrophic lateral sclerosis case carrying VCP Arg487His mutation with a unique TDP-43 proteinopathy.

MLA

Matsubara, Tomoyasu, et al. “An Autopsy Report of a Familial Amyotrophic Lateral Sclerosis Case Carrying VCP Arg487His Mutation with a Unique TDP-43 Proteinopathy.” Neuropathology : Official Journal of the Japanese Society of Neuropathology, vol. 41, no. 2, Apr. 2021, pp. 118–26. EBSCOhost, https://doi.org/10.1111/neup.12710.

APA

Matsubara, T., Izumi, Y., Oda, M., Takahashi, M., Maruyama, H., Miyamoto, R., Watanabe, C., Tachiyama, Y., Morino, H., Kawakami, H., Saito, Y., & Murayama, S. (2021). An autopsy report of a familial amyotrophic lateral sclerosis case carrying VCP Arg487His mutation with a unique TDP-43 proteinopathy. Neuropathology : Official Journal of the Japanese Society of Neuropathology, 41(2), 118–126. https://doi.org/10.1111/neup.12710

Chicago

Matsubara, Tomoyasu, Yuishin Izumi, Masaya Oda, Masatoshi Takahashi, Hirofumi Maruyama, Ryosuke Miyamoto, Chigusa Watanabe, et al. 2021. “An Autopsy Report of a Familial Amyotrophic Lateral Sclerosis Case Carrying VCP Arg487His Mutation with a Unique TDP-43 Proteinopathy.” Neuropathology : Official Journal of the Japanese Society of Neuropathology 41 (2): 118–26. doi:10.1111/neup.12710.