FKBP10 Variants: Differentiation Between Bruck Syndrome Type 1 And Osteogenesıs Imperfecta Type XI
J Clin Res Pediatr Endocrinol. 2025 Nov 17. doi: 10.4274/jcrpe.galenos.2025.2025-8-4. Online ahead of print. ABSTRACT Biallelic FKBP10 variants cause autosomal recessive osteogenesis imperfecta(OI) type XI …