CHARACTERIZING THE ROLE OF ABCG5/G8 IN SITOSTEROLEMIA: DIAGNOSTIC CHALLENGES IN DIFFERENTIATING FROM FAMILIAL HYPERCHOLESTEROLEMIA
10905 10063 10064 8448 3566 3539 3545 3552 5 2024 10.34689/SH.2024.26.5.018 Introduction. Sitosterolemia is a rare genetic disorder directly associated with dysfunction of ABCG5 and G8 genes. The data obtained was used to analyze the cellular mechanisms and the role of transporters in absorption and excretion of serum sterols. Thus, to understand ...
Изменен: 31.10.2024Путь: Главная / Home / Publications
CHARACTERIZING THE ROLE OF ABCG5/G8 IN SITOSTEROLEMIA: DIAGNOSTIC CHALLENGES IN DIFFERENTIATING FROM FAMILIAL HYPERCHOLESTEROLEMIA
5 2024
Изменен: 31.10.2024Путь: Главная / Публикации
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