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Familial chylomicronemia syndrome (FCS), also referred to as type 1 hyperlipoproteinemia or lipoprotein lipase deficiency, is a rare genetic lipid disorder characterized by severe elevations in cir... Click to show full abstract
Familial chylomicronemia syndrome (FCS), also referred to as type 1 hyperlipoproteinemia or lipoprotein lipase deficiency, is a rare genetic lipid disorder characterized by severe elevations in cir...
Keywords:
building better;
familial chylomicronemia;
better understanding;
chylomicronemia syndrome
Journal Title: Expert Review of Clinical Pharmacology
Year Published: 2017
Link to full text (if available)
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Journal Title: Expert Review of Clinical Pharmacology
Year Published: 2017
Link to full text (if available)
Share on Social Media: Sign Up to like & get
recommendations!