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Activating Mutations of the G-protein Subunit α (11) Interdomain Interface Cause Autosomal Dominant Hypocalcemia Type 2
CONTEXT: Autosomal dominant hypocalcemia types 1 and 2 (ADH1 and ADH2) are caused by germline gain-of-function mutations of the calcium-sensing receptor (CaSR) and its signaling partner, the G-protein subunit α (11) (Gα (11)), respectively. More than 70 different gain-of-function CaSR mutations, but...
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| 出版年: | J Clin Endocrinol Metab |
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| 主要な著者: | , , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2019
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7048683/ https://ncbi.nlm.nih.gov/pubmed/31820785 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/clinem/dgz251 |
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