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Updated: Jul 9, 2026

A Familial Hypercholesterolemia Human Liver Chimeric Mouse Model Using Induced Pluripotent Stem Cell-derived Hepatocytes
Published on: September 15, 2018
Familial chylomicronemia syndrome
M K Mohandas1, J Jemila, A S Ajith Krishnan
1Department of Ophthalmology, Medical College, Thiruvananthapuram, Kerala, India. bdbenroy@yahoo.com
Abstract:
Familial chylomicronemia syndrome is a group of rare genetic disorders characterized by deficient activity of an enzyme lipoprotein lipase or apo-protein C-II deficiency. Incidence is 1 out of 1,000,000. Alternative names to this syndrome are Type I hyper lipoproteinemia and familial lipoprotein lipase deficiency.
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