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Pharmacological management of X‐linked hypophosphataemia
The most common heritable disorder of renal phosphate wasting, X‐linked hypophosphataemia (XLH), was discovered to be caused by inactivating mutations in the phosphate regulating gene with homology to endopeptidases on the X‐chromosome (PHEX) gene in 1995. Although the exact molecular mechanisms by...
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| Pubblicato in: | Br J Clin Pharmacol |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
John Wiley and Sons Inc.
2018
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6533442/ https://ncbi.nlm.nih.gov/pubmed/30207609 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/bcp.13763 |
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