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Familial Chylomicronemia Syndrome With a Novel Homozygous LPL Mutation Identified in Three Siblings in Their 50s
Familial Chylomicronemia Syndrome With a Novel Homozygous LPL Mutation Identified in Three Siblings in Their 50s
2019
Masako Ueda
Frances M. Burke
Alan T. Remaley
Robert A. Hegele
Daniel J. Rader
Richard L. Dunbar
Keywords:
Familial Chylomicronemia
Mutation
Cardiology
Pediatrics
Internal medicine
Diabetes mellitus
Medicine
Hyperlipidemia
Genetics
drug administration
Hepatosplenomegaly
Familial lipoprotein lipase deficiency
lipoprotein metabolism
Correction
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