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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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Bibliografski detalji
Glavni autori: Fu, Jiao, Dumitrescu, Alexandra M.
Format: Artigo
Jezik:Inglês
Izdano: 2013
Teme:
Online pristup: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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