Cargando...
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...
Guardado en:
| Publicado en: | Eur J Endocrinol |
|---|---|
| Autores principales: | , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
2020
|
| Materias: | |
| Acceso en línea: | 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 |
| Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|