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 <i>ABCG5</i> or <i>ABCG8</i>. <i>ABCG5 ABCG8</i> encodes a pair of ABC half transporters that form a heterodimer (G5G8),...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2021-03-01
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| Series: | International Journal of Molecular Sciences |
| Subjects: | |
| Online Access: | https://www.mdpi.com/1422-0067/22/5/2641 |