ArticleOrphanet journal of rare diseases2021
Clinical, molecular and glycophenotype insights in SLC39A8-CDG.
Eleonora Bonaventura et al.PubMed ↗Full text ↗Publisher ↗
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ArticleOrphanet journal of rare diseases2021
Eleonora Bonaventura et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.