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Publication Detail
Neuropathological findings from a human post mortem case of distal hereditary motor neuropathy (dHMN) due to p.Ser135Phe HSPB1 mutation and transgenic mice with mutant or wild-type HSP27 overexpression
Abstract
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Department of Neuromuscular Diseases
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Department of Neuromuscular Diseases
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Department of Neuromuscular Diseases
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UCL Queen Square Institute of Neurology
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Department of Neuromuscular Diseases
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Department of Neuromuscular Diseases
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