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First Report of Familial Dysalbuminemic Hyperthyroxinemia With an ALB Variant
Familial dysalbuminemic hyperthyroxinemia (FDH) is an inherited disease characterized by increased circulating total thyroxine (T4) levels and normal physiological thyroid function. Heterozygous albumin gene (ALB) variants have been reported to be the underlying cause of FDH. To our knowledge, there...
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| 出版年: | Ann Lab Med |
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| 主要な著者: | , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
The Korean Society for Laboratory Medicine
2017
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5107620/ https://ncbi.nlm.nih.gov/pubmed/27834068 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3343/alm.2017.37.1.63 |
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