A truncating SOD1 mutation, p.Gly141X, is associated with clinical and pathologic heterogeneity, including frontotemporal lobar degeneration

Masataka Nakamura, Kevin F. Bieniek, Wen Lang Lin, Neill R. Graff-Radford, Melissa E. Murray, Monica Castanedes-Casey, Pamela Desaro, Matthew C. Baker, Nicola J. Rutherford, Janice Robertson, Rosa Rademakers, Dennis W. Dickson, Kevin B. Boylan

Research output: Contribution to journal › Article › peer-review

12 Scopus citations

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