Nuclear lamina invaginations are not a pathological feature of C9orf72 ALS/FTD
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ID: 267556
2021
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Abstract
The most common genetic cause of familial and sporadic amyotrophic lateral sclerosis (ALS) is a GGGGCC hexanucleotide repeat expansion (HRE) in the C9orf72 gene. While direct molecular hallmarks of the C9orf72 HRE (repeat RNA foci, dipeptide repeat protein ...
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| Reference Key |
rothstein2021actanuclear
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|---|---|
| Authors | Alyssa N. Coyne, Jeffrey D. Rothstein;Alyssa N. Coyne;Jeffrey D. Rothstein; |
| Journal | acta neuropathologica communications |
| Year | 2021 |
| DOI |
10.1186/s40478-021-01150-5
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| URL | |
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