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Q41341998-847C899D-1529-4EC5-9581-4D8E847121C7
Q41341998-847C899D-1529-4EC5-9581-4D8E847121C7
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Statement
http://www.wikidata.org/entity/statement/Q41341998-847C899D-1529-4EC5-9581-4D8E847121C7
Inclusions in frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP) and amyotrophic lateral sclerosis (ALS), but not FTLD with FUS proteinopathy (FTLD-FUS), have properties of amyloid.
P2860
Q41341998-847C899D-1529-4EC5-9581-4D8E847121C7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41341998-847C899D-1529-4EC5-9581-4D8E847121C7
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Statement
wasDerivedFrom
ce2e439b1baf7402be65f0809fd7f2aff1ac772d
P2860
An ALS-associated mutation affecting TDP-43 enhances protein aggregation, fibril formation and neurotoxicity