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注意:仅列出部分参考文献,下载原文获取全部文献信息。Oligodendrogliopathy in neurodegenerative diseases with abnormal protein aggregates: The forgotten partner
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Sporadic four-repeat tauopathy with frontotemporal degeneration, parkinsonism and motor neuron disease
YS Piao et al.
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JJ Zarranz et al.
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I Ferrer et al.
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