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ArticleEndocrine connections2024

Endocrinological features and epileptic encephalopathy in COX deficiency due to SCO1 mutations: case series and review of literature.

Alessandro Barbato et al.PubMed ↗Full text ↗Publisher ↗

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3 papers cite it

2024
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2026
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Full record →Abstract, authors, funding and every citing paper · PMID 39214134