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Control of PTH secretion by the TRPC1 ion channel
Familial hypocalciuric hypercalcemia (FHH) is a genetic condition associated with hypocalciuria, hypercalcemia, and, in some cases, inappropriately high levels of circulating parathyroid hormone (PTH). FHH is associated with inactivating mutations in the gene encoding the Ca(2+)-sensing receptor (Ca...
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| Yayımlandı: | JCI Insight |
|---|---|
| Asıl Yazarlar: | , , , , , , , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
American Society for Clinical Investigation
2020
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7205425/ https://ncbi.nlm.nih.gov/pubmed/32213715 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/jci.insight.132496 |
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