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Mutations in the SPTLC1 gene are a cause of juvenile amyo... | ResearchHub
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Mutations in the SPTLC1 gene are a cause of juvenile amyotrophic lateral sclerosis that may be amenable to serine supplementation
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Authors
Jamlik-Omari Johnson
•
Jamlik-Omari Johnson
66 more
•
Bryan Traynor
Published
June 29, 2020
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Preprint Server
Topics
Bioinformatics
Internal Medicine
Endocrinology
Neurology
Genetics And Genomics
Biology
Bioinformatics
Medicine
Internal Medicine
Endocrinology
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DOI
10.1101/770339
License
CC0
