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Inherited defects in thyroid hormone cell-membrane transport and metabolism
The description of two novel human defects in the last ten years has uncovered new aspects of thyroid hormone physiology with regard to cellular-membrane transport and intracellular metabolism. Mutations in the X-linked monocarboxylate transporter 8 (MCT8) gene result in an invalidating neurodevelop...
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| Asıl Yazarlar: | , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2013
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3959653/ https://ncbi.nlm.nih.gov/pubmed/24629861 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.beem.2013.05.014 |
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