CHARACTERIZING THE ROLE OF ABCG5/G8 IN SITOSTEROLEMIA: DIAGNOSTIC CHALLENGES IN DIFFERENTIATING FROM FAMILIAL HYPERCHOLESTEROLEMIA
... 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... ... disease. Aim. To investigate the clinical manifestation between sitosterolemia and familial hypercholesterolemia (FH), focusing on how dysfunctions of transporters lead... ... manifest cardiovascular complications with elevated total cholesterol (TC) levels. The lipid profile distinguishes these conditions, necessitating HPLC, GC-MS tools. Genetic...
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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