טוען...
Insights into molecular properties of the human monocarboxylate transporter 8 by combining functional with structural information
BACKGROUND: The monocarboxylate transporter 8 (MCT8) is a member of the major facilitator superfamily (MFS) and transports specificly iodothyronines. MCT8 mutations are the underlying cause of a syndrome of severe X-linked psychomotor retardation known as the Allan-Herndon-Dudley syndrome. This synd...
שמור ב:
| Main Authors: | , , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
BioMed Central
2011
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3155110/ https://ncbi.nlm.nih.gov/pubmed/21835051 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1756-6614-4-S1-S4 |
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