Clinicopathologic study on an ALS family with a heterozygous E478G optineurin mutation.
Ito H; Nakamura M; Komure O; Ayaki T; Wate R; Maruyama H; Nakamura Y; Fujita K; Kaneko S; Okamoto Y; Ihara M; Konishi T; Ogasawara K; Hirano A; Kusaka H; Kaji R; Takahashi R; Kawakami H; Acta Neuropathologica, 2011, vol. 122, issue 2, p 223, ISSN 14320533. ISBN 14320533.

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