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GLT8D1 mutations cause amyotrophic lateral sclerosis via ... | ResearchHub
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GLT8D1 mutations cause amyotrophic lateral sclerosis via disruption of neurotrophin signalling within membrane lipid rafts
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Authors
Tobias Moll
11 more
Tobias Moll
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Emily Graves
9 more
•
Pamela Shaw
Published
July 1, 2022
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Topics
Biology
Neuroscience
Chemistry
Medicine
Internal Medicine
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DOI
10.1101/2022.06.28.497990
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cc-no
Supporters
Support the authors with ResearchCoin
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Preprint Server
Topics
Biology
Neuroscience
Chemistry
Medicine
Internal Medicine
Show all topics
DOI
10.1101/2022.06.28.497990
License
cc-no
