Wikidata

(Q41341998)

English

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.

scientific article published on 3 February 2013

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Statements

title
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 (English)
1 reference
stated in
Europe PubMed Central
PMCID
3593646
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23378033%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 February 2020
cites work

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