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Bone Geometry and Microarchitecture Deficits in Children with Alagille Syndrome
Alagille syndrome (ALGS) is an autosomal dominant disorder attributed to mutations in the Notch signaling pathway. Children with ALGS are at increased risk for fragility fracture of unknown etiology. Our objective was to characterize bone mass, geometry, and microarchitecture in children with ALGS....
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| Publicado no: | Bone |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7680312/ https://ncbi.nlm.nih.gov/pubmed/32791330 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bone.2020.115576 |
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