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Prosthetic rehabilitation of a young patient with Hypophosphatasia – A review and case report
Hypophosphatasia is a congenital disease characterized by deficiency of serum and tissue non-specific alkaline phosphatase activity. The disease occurs due to mutations in the liver/bone/kidney alkaline phosphatase gene. Six clinical forms of hypophosphatasia are recognized. Systemic symptoms of the...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2012
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3341764/ https://ncbi.nlm.nih.gov/pubmed/22557902 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0976-237X.94551 |
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