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Mice with endogenous TDP‐43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis | The EMBO Journal
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Frontiers | A C-Terminally Truncated TDP-43 Splice Isoform Exhibits Neuronal Specific Cytoplasmic Aggregation and Contributes to TDP-43 Pathology in ALS
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Mice with endogenous TDP‐43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis | The EMBO Journal
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Domain structures and assembly of TDP-43 proteins. (A) TDP-43 has two... | Download Scientific Diagram
A. Schematic representation of the primary structural architecture of... | Download Scientific Diagram
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