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Dental effects of enzyme replacement therapy in case of childhood-type hypophosphatasia
BACKGROUND: Hypophosphatasia (HPP), a skeletal disease characterized by hypomineralization of bone and teeth, is caused by an ALPL gene mutation that leads to low activity of the tissue non-specific alkaline phosphatase enzyme. Although enzyme replacement therapy (ERT) was recently introduced for af...
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| Publicado no: | BMC Oral Health |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8237502/ https://ncbi.nlm.nih.gov/pubmed/34176466 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12903-021-01673-2 |
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