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BioWorld - Wednesday, November 27, 2024
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» Researchers identify SPTSSA gene variants to impact hereditary spastic paraplegia risk
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Biomarkers
Researchers identify SPTSSA gene variants to impact hereditary spastic paraplegia risk
Nov. 2, 2022
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The Undiagnosed Diseases Network uncovered three unrelated individuals with mutations in the gene encoding serine palmitoyltransferase small subunit A (SPTSSA).
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