Intranasal delivery of Thyroid hormones in MCT8 deficiency

Loss of function mutations in the gene encoding the thyroid hormone transporter monocarboxylate transporter 8 (MCT8) lead to severe neurodevelopmental defects in humans associated with a specific thyroid hormone phenotype manifesting high serum 3,5,3’-triiodothyronine (T3) and low thyroxine (T4) lev...

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Detaylı Bibliyografya
Yayımlandı:PLoS One
Asıl Yazarlar: Grijota-Martínez, Carmen, Bárez-López, Soledad, Ausó, Eva, Refetoff, Samuel, Frey, William H., Guadaño-Ferraz, Ana
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Public Library of Science 2020
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7371167/
https://ncbi.nlm.nih.gov/pubmed/32687511
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0236113
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