FUS P525L mutation causing amyotrophic lateral sclerosis and movement disorders
Author:
Affiliation:
1. Department of Neurology The First Affiliated Hospital of Nanchang University Nanchang China
2. Department of Diagnostic Center Ascension Seton Medical Center Austin Austin TX USA
Funder
National Natural Science Foundation of China
Publisher
Wiley
Subject
Behavioral Neuroscience
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/brb3.1625
Reference34 articles.
1. Juvenile ALS with basophilic inclusions is a FUS proteinopathy with FUS mutations
2. FUS mutations in amyotrophic lateral sclerosis: clinical, pathological, neurophysiological and genetic analysis
3. FUS: A new actor on the frontotemporal lobar degeneration stage
4. Novel genes associated with amyotrophic lateral sclerosis: diagnostic and clinical implications
5. Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation
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