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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2021
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7961684/ https://www.ncbi.nlm.nih.gov/pubmed/33807969 http://dx.doi.org/10.3390/ijms22052641 |