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ArticleAmerican journal of human genetics2024

De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features.

Sureni V Mullegama et al.PubMed ↗Full text ↗Publisher ↗

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1 paper cites it

2024
2025
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Full record →Abstract, authors, funding and every citing paper · PMID 38531365