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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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| Yayımlandı: | PLoS One |
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| Asıl Yazarlar: | , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Public Library of Science
2020
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| Konular: | |
| 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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