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Abnormal thyroid hormone metabolism in mice lacking the monocarboxylate transporter 8
In humans, inactivating mutations in the gene of the thyroid hormone transporter monocarboxylate transporter 8 (MCT8; SLC16A2) lead to severe forms of psychomotor retardation combined with imbalanced thyroid hormone serum levels. The MCT8-null mice described here, however, developed without overt de...
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society for Clinical Investigation
2007
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1797602/ https://ncbi.nlm.nih.gov/pubmed/17318265 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI28253 |
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