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Updated: Mar 1, 2026

A Familial Hypercholesterolemia Human Liver Chimeric Mouse Model Using Induced Pluripotent Stem Cell-derived Hepatocytes
Published on: September 15, 2018
Fenotipo variable asociado con mutaciones compuestas del gen LDLR en pacientes con hipercolesterolemia familiar:
Noor Alicezah Mohd Kasim1,2, Yung-An Chua1,3, Siti Hamimah Sheikh Abdul Kadir1,3
1Cardiovascular Advancement and Research Excellence Institute (CARE Institute), Universiti Teknologi MARA, Selangor, Malaysia.
La hipercolesterolemia familiar homocigótica (HoFH) puede presentarse con síntomas variables debido a mutaciones compuestas del gen del receptor de lipoproteínas de baja densidad (LDLR). Las nuevas variantes de LDLR en el exón 18 pueden provocar una hipercolesterolemia más leve y características clínicas atípicas en pacientes con HoFH.
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