A comprehensive report of the clinical and mutational profiles of 30 Iranian malignant infantile osteopetrosis patients
Osteopetrosis is a group of genetically and clinically diverse inherited disorders characterized by an increase in bone density. The main known cause is an abnormality in the development or function of osteoclasts. Hence, the process of bone resorption is impaired, resulting in: 1- a reduction in bo...
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| Hoofdauteurs: | , , , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Elsevier
2025-02-01
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| Reeks: | Molecular and Cellular Probes |
| Onderwerpen: | |
| Online toegang: | http://www.sciencedirect.com/science/article/pii/S0890850825000076 |
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