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Familial hypocalciuric hypercalcemia and related disorders
Familial hypocalciuric hypercalcemia (FHH) causes hypercalcemia by three genetic mechanisms: inactivating mutations in the calcium-sensing receptor, the G-protein subunit α(11), or adaptor-related protein complex 2, sigma 1 subunit. While hypercalcemia in other conditions causes significant morbidit...
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| Gepubliceerd in: | Best Pract Res Clin Endocrinol Metab |
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| Hoofdauteurs: | , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2018
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6767927/ https://ncbi.nlm.nih.gov/pubmed/30449544 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.beem.2018.05.004 |
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