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Osteoclastogenesis inhibition by mutated IGSF23 results in human osteopetrosis
OBJECTIVES: Osteopetrosis is a rare inherited skeletal disease characterized by increased bone mineral density due to the loss of osteoclast function or differentiation potential. MATERIALS AND METHODS: The study involved a Chinese patient with osteopetrosis (the proband) and her immediate family me...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2019
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6869366/ https://www.ncbi.nlm.nih.gov/pubmed/31560140 http://dx.doi.org/10.1111/cpr.12693 |