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Sitosterolemia: Twenty Years of Discovery of the Function of ABCG5 ABCG8
Sitosterolemia is a lipid disorder characterized by the accumulation of dietary xenosterols in plasma and tissues caused by mutations in either ABCG5 or ABCG8. ABCG5 ABCG8 encodes a pair of ABC half transporters that form a heterodimer (G5G8), which then traffics to the surface of hepatocytes and en...
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| Publicado no: | Int J Mol Sci |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7961684/ https://ncbi.nlm.nih.gov/pubmed/33807969 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms22052641 |
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