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. (Q41341998)
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scientific article published on 3 February 2013
| Language | Label | Description | Also known as |
|---|---|---|---|
| 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 |
Statements
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)
Marsel Mesulam
Changiz Geula
Jane Y Wu
Esther N Bit-Ivan
Rakhee Ganti
Melanie Peterson
Nailah Siddique
3 February 2013