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Should all patients with hyperparathyroidism be screened for a CDC73 mutation?
Primary hyperparathyroidism (PH) is a common endocrine abnormality and may occur as part of a genetic syndrome. Inactivating mutations of the tumour suppressor gene CDC73 have been identified as accounting for a large percentage of hyperparathyroidism-jaw tumour syndrome (HPT-JT) cases and to a less...
Tallennettuna:
| Julkaisussa: | Endocrinol Diabetes Metab Case Rep |
|---|---|
| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Bioscientifica Ltd
2018
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5843797/ https://ncbi.nlm.nih.gov/pubmed/29535865 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1530/EDM-17-0164 |
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