A rare inherited inborn error of metabolism involving the absence of the enzyme called lipoprotein lipase which results in increased blood triglyeride and chylomicron levels. See also Familial hyperchylomicronemia
Chemwatch helps thousands of organisations manage chemical safety. Book a free demo to see how.
As scientists who evolve with technology we treat innovation as a way of life, a life we dedicate to improvement and advancement of Safety, Health and Environment.
