Associated Papers
Presentation of Rare Phenotypes Associated with the FKBP10 Gene.
Merkuryeva ES et al.
Genes, 2024
Novel mutation of FKBP10 in a pediatric patient with osteogenesis imperfecta type XI identified by clinical exome sequencing.
Velasco HM et al.
The Application of Clinical Genetics, 2017
Novel FKBP10 Mutation in a Patient with Osteogenesis Imperfecta Type XI.
Seyedhassani SM et al.
Fetal and Pediatric Pathology, 2016
Select a paper to view details