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Oxford University Press

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TDP-43 proteinopathy: the neuropathology underlying major forms of sporadic and familial frontotemporal lobar degeneration and motor neuron disease

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Regulation of Gene Expression by TDP-43 and FUS/TLS in Frontotemporal Lobar Degeneration

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Absence of heterogeneous nuclear ribonucleoproteins and survival motor neuron protein in TDP-43 positive inclusions in frontotemporal lobar degeneration

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