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].
作者信息
Abdulmalek Omar, Alrefaie Khadeja
机构信息
University of Glasgow, United Kingdom.
Royal College of Surgeons in Ireland, Bahrain.
出版信息
Heliyon. 2024 Nov 19;10(22):e40336. doi: 10.1016/j.heliyon.2024.e40336. eCollection 2024 Nov 30.
Abstract
摘要
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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].
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本文引用的文献
1
A novel compound heterozygous variation in the gene causes Bruck syndrome without congenital contractures: A case report.该基因中的一种新型复合杂合变异导致无先天性挛缩的布鲁克综合征：一例报告。
Heliyon. 2024 Mar 22;10(7):e28680. doi: 10.1016/j.heliyon.2024.e28680. eCollection 2024 Apr 15.
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