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ArticleHeliyon2024

Letter to the editor of Heliyon re: A novel compound heterozygous variation in the FKBP10 gene causes Bruck syndrome without congenital contractures: A case report [Heliyon 2024; 10(7): e28680].

Omar Abdulmalek et al.PubMed ↗Full text ↗Publisher ↗

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Full record →Abstract, authors, funding and every citing paper · PMID 39641041