Associated Papers
Osteoclast-independent osteocyte dendrite defects in mice bearing the osteogenesis imperfecta-causing Sp7 R342C mutation.
Wang JS et al.
Bone Research, 2025
Update on the Genetics of Osteogenesis Imperfecta.
Jovanovic M et al.
Calcified Tissue International, 2024
A homozygous SP7/OSX mutation causes osteogenesis and dentinogenesis imperfecta with craniofacial anomalies.
Al-Mutairi DA et al.
Jbmr Plus, 2024
Long-term follow-up of severe autosomal recessive SP7-related bone disorder.
Gauthier LW et al.
Bone, 2024
Dominant osteogenesis imperfecta with low bone turnover caused by a heterozygous SP7 variant.
Ludwig K et al.
Bone, 2022
Select a paper to view details