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Non-autoimmune subclinical hypothyroidism due to a mutation in TSH receptor: report on two brothers
Subclinical hypothyroidism (SH) is a condition characterized by a mild persistent thyroid failure. The main cause is represented by autoimmune thyroiditis, but mutations in genes encoding proteins involved in TSH pathway are thought to be responsible for SH, particularly in cases arising in familial...
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| Autors principals: | , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2013
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3565903/ https://ncbi.nlm.nih.gov/pubmed/23332130 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1824-7288-39-5 |
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