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Mutations in proteasome-related genes are associated with thyroid hemiagenesis
PURPOSE: Human thyroid development is a complex and still unexplained process. Thyroid hemiagenesis is a congenital anomaly, where one of the thyroid lobes fails to develop. In the majority of patients with thyroid hemiagenesis, the genetic background remains unknown. The aim of the study was to sea...
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| 出版年: | Endocrine |
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| 主要な著者: | , , , , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Springer US
2017
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5395596/ https://ncbi.nlm.nih.gov/pubmed/28390009 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12020-017-1287-4 |
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