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Sporadic Nonautoimmune Neonatal Hyperthyroidism Due to A623V Germline Mutation in the Thyrotropin Receptor Gene
Neonatal hyperthyroidism is a rare disorder and occurs in two forms. An autoimmune form is associated with maternal Graves' disease, resulting from transplacental passage of maternal thyroid−stimulating antibodies and a nonautoimmune form is caused by gain of function mutations in the thyrotrop...
| Autores principales: | , , , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
Galenos Publishing
2010
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3005687/ https://www.ncbi.nlm.nih.gov/pubmed/21274318 http://dx.doi.org/10.4274/jcrpe.v2i4.168 |