Generation of skin-derived iPSCs from an Osteogenesis imperfecta patient carrying WNT1(c.677C>T) mutation
pubmed: wnt1 2024-04-27
Summary:
CONCLUSION: A patient-specific WNT1 gene mutation (WNT1^(c.677C>T)) iPSC line was established, which can provide a cell model for the study of OI caused by the mutation.