Long-Read Sequencing Unlocks Rare Genetic Cause of Inherited Ataxia
Researchers used long-read genome sequencing and RNA analysis to diagnose a rare hereditary ataxia caused by biallelic VPS41 variants, expanding ...
Researchers used long-read genome sequencing and RNA analysis to diagnose a rare hereditary ataxia caused by biallelic VPS41 variants, expanding ...
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© 2025 Scienmag - Science Magazine