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Molecular genetics in primary hyperparathyroidism: the role of genetic tests in differential diagnosis, disease prevention strategy, and therapeutic planning. A 2017 update
Primary hyperparathyroidism (PHPT) is one of the most frequent endocrine disease in developed countries. It mainly occurs as sporadic cases (about 90–95% of cases), while only the remaining 5–10% is represented by familial inherited parathyroid disorders due to causative mutations in specific target...
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| Publicado no: | Clin Cases Miner Bone Metab |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
CIC Edizioni Internazionali
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5505716/ https://ncbi.nlm.nih.gov/pubmed/28740527 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11138/ccmbm/2017.14.1.060 |
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