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ArticleGenetics in medicine : official journal of the American College of Medical Genetics2024

Dominant missense variants in SREBF2 are associated with complex dermatological, neurological, and skeletal abnormalities.

Matthew J Moulton et al.PubMed ↗Full text ↗Publisher ↗

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2024
2025
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Full record →Abstract, authors, funding and every citing paper · PMID 38847193