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Functional and Molecular Characterization of New SPTLC1 M... | ResearchHub
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Functional and Molecular Characterization of New SPTLC1 Missense Variants in Patients with Hereditary Sensory and Autonomic Neuropathy Type 1 (HSAN1)
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Authors
Julie Rochat
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Julie Rochat
•
André Blavier
11 more
•
David Cheillan
Published
May 26, 2024
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Journal
Genes
Topics
Biology
Physiology
Cellular And Molecular Neuroscience
Cell Biology
Phenotype
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DOI
10.3390/genes15060692
License
CC-BY
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Supporters
Support the authors with ResearchCoin
Tip RSC
Journal
Genes
Topics
Biology
Physiology
Cellular And Molecular Neuroscience
Cell Biology
Phenotype
Show all topics
DOI
10.3390/genes15060692
License
CC-BY
Other Formats
PDF