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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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| Publicat a: | Medicine (Baltimore) |
|---|---|
| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Lippincott Williams & Wilkins
2020
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| Matèries: | |
| Accés en línia: | 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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