Associated Papers
Clinical features and molecular characterization of Chinese patients with FKBP10 variants.
Tan Z et al.
Molecular Genetics & Genomic Medicine, 2023
Novel mutations in FKBP10 in Chinese patients with osteogenesis imperfecta and their treatment with zoledronic acid.
Xu XJ et al.
Journal of Human Genetics, 2017
Select a paper to view details