ArticleJCI insight2025
A hypomorphic Mpi mutation unlocks an in vivo tool for studying global N-glycosylation deficiency.
Elisa B Lin et al.PubMed ↗Full text ↗Publisher ↗
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ArticleJCI insight2025
Elisa B Lin et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.