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Recurrent EZH1 mutations are a second hit in autonomous thyroid adenomas
Autonomous thyroid adenomas (ATAs) are a frequent cause of hyperthyroidism. Mutations in the genes encoding the TSH receptor (TSHR) or the Gs protein α subunit (GNAS) are found in approximately 70% of ATAs. The involvement of other genes and the pathogenesis of the remaining cases are presently unkn...
Guardat en:
| Publicat a: | J Clin Invest |
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| Autors principals: | , , , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Society for Clinical Investigation
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5004945/ https://ncbi.nlm.nih.gov/pubmed/27500488 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI84894 |
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