FK506-binding protein-65(English)

• defect causes types X and XI osteogenesis imperfecta via aberrant collagen crosslinking, folding, and chaperoning
• IFITM, LEPRE1, MMTV, OASIS, OI, PEDF, PPIB, P3H1, TRIC-B, BMP1, BRIL, CRTAP, CyPB, EDS, HSP47
• Skeleton and bone (formation), Genetics, Pediatrics
• https://doi.org…000000000000117