Associated Papers
Paradoxical combination of osteosclerosis and osteopenia in an adult woman with biallelic TNFRSF11A loss-of-function variants escaping nonsense-mediated decay.
Gajewski D et al.
Jbmr Plus, 2025
A Null Mutation of TNFRSF11A Causes Dysosteosclerosis, Not Osteopetrosis.
Kırkgöz T et al.
Frontiers in Genetics, 2022
Genetic disorders associated with the RANKL/OPG/RANK pathway.
Xue JY et al.
Journal of Bone and Mineral Metabolism, 2021
Dysosteosclerosis is also caused by TNFRSF11A mutation.
Guo L et al.
Journal of Human Genetics, 2018
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