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Familial dysalbuminaemic hyperthyroxinaemia interferes with current free thyroid hormone immunoassay methods
OBJECTIVE: Familial dysalbuminaemic hyperthyroxinaemia (FDH), most commonly due to an Arginine to Histidine mutation at residue 218 (R218H) in the albumin gene, causes artefactual elevation of free thyroid hormones in euthyroid individuals. We have evaluated the susceptibility of most current free t...
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| Publicat a: | Eur J Endocrinol |
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| Autors principals: | , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Bioscientifica Ltd
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7222281/ https://ncbi.nlm.nih.gov/pubmed/32213658 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1530/EJE-19-1021 |
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