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Matthew Nolan et al.
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Kai Y. Soo et al.
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Mariko Ogawa et al.
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Brian D. Freibaum et al.
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Julie D. Atkin et al.
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Hyder Ali Khan et al.
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Ataxin-2 interacts with FUS and intermediate-length polyglutamine expansions enhance FUS-related pathology in amyotrophic lateral sclerosis
Manal A. Farg et al.
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Caroline Vance et al.
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P. Bernardoni et al.
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FET proteins in frontotemporal dementia and amyotrophic lateral sclerosis
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Kylie M. Wagstaff et al.
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Harro Seelaar et al.
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Ian P. Blair et al.
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D. Baeumer et al.
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Joel C. Watts et al.
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Saya Nakagomi et al.
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S. Bolte et al.
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R Fujii et al.
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Domain Architectures and characterization of an RNA-binding protein, TLS
Y Iko et al.
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A Mezzacasa et al.
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RP VanderWaal et al.
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