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Thyroid hormone resistance syndrome with P453T mutation in thyroid hormone receptor β gene: A pedigree report
RATIONALE: Thyroid hormone resistance syndrome (THRS) is an inherited condition characterized by reduced responsiveness of target tissues to thyroid hormone. Due to their nonspecific symptomatic manifestations, these patients can be misdiagnosed. This study reports a pedigree with THRS caused by a m...
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| 出版年: | Medicine (Baltimore) |
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| 主要な著者: | , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Lippincott Williams & Wilkins
2020
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7598850/ https://ncbi.nlm.nih.gov/pubmed/33126322 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000022824 |
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