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Ethical issues in managing Lysosomal storage disorders in children in low and middle income countries
The lysosomal storage diseases are a group of rare, inherited metabolic diseases affecting about 1 in 7000 to 8000 people. In recent years, the introduction of enzyme replacement therapy, substrate reduction therapy and small molecule therapy, has changed the natural course of this otherwise progres...
Uloženo v:
| Vydáno v: | Pak J Med Sci |
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| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Professional Medical Publications
2017
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5648935/ https://ncbi.nlm.nih.gov/pubmed/29067088 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12669/pjms.334.12975 |
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