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Recombinant human parathyroid hormone (1–84) is effective in CASR-associated hypoparathyroidism
INTRODUCTION: Gain-of-function mutations in the CASR gene cause Autosomal Dominant Hypocalcemia Type 1 (ADH1), the most common genetic cause of isolated hypoparathyroidism. Subjects have increased calcium sensitivity in the renal tubule, leading to increased urinary calcium excretion, nephrocalcinos...
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| Publicat a: | Eur J Endocrinol |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7853300/ https://ncbi.nlm.nih.gov/pubmed/33112267 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1530/EJE-20-0710 |
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