Slow disease progression and characteristic TDP‐43 inclusions in a patient with familial amyotrophic lateral sclerosis carrying a <i>TARDBP</i> G357S variant-Reference-Cited by-同舟云学术

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Slow disease progression and characteristic TDP‐43 inclusions in a patient with familial amyotrophic lateral sclerosis carrying a TARDBP G357S variant

Published:2024-02 Issue:1 Volume:50 Page:
ISSN:0305-1846
Container-title:Neuropathology and Applied Neurobiology
language:en
Short-container-title:Neuropathology Appl Neurobio

Author:

Sainouchi Makoto¹,Oginezawa Shinya²,Tada Mari¹^ORCID,Ishihara Tomohiko²³,Onodera Osamu²,Kakita Akiyoshi¹

Affiliation:

1. Department of Pathology, Brain Research Institute Niigata University Niigata Japan

2. Department of Neurology, Brain Research Institute Niigata University Niigata Japan

3. Advanced Treatment of Neurological Diseases Branch, Endowed Research Branch, Brain Research Institute Niigata University Niigata Japan

Funder

Japan Society for the Promotion of Science

Ministry of Health, Labour and Welfare

Publisher

Wiley

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/nan.12966

Reference17 articles.

1. RRM adjacent TARDBP mutations disrupt RNA binding and enhance TDP-43 proteinopathy

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