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A new family with an activating mutation (G431S) in the TSH receptor gene: a phenotype discussion and review of the literature
Germline nonautoimmune hyperthyroidism due to an activating mutation in the thyroid stimulating hormone receptor gene is an uncommon disease. To date 32 different mutations have been described. The severity of the hyperthyroid symptoms is variable and phenotype differences have been described in sub...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2014
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4396564/ https://www.ncbi.nlm.nih.gov/pubmed/25873976 http://dx.doi.org/10.1186/1687-9856-2014-23 |