Genetic diagnosis of familial hypercholesterolemia in Han Chinese

Abstract Familial hypercholesterolemia (FH) is an inherited autosomal dominant disorder of lipoprotein metabolism resulting in elevated serum levels of low-density lipoprotein cholesterol (LDL-C), which lead to increased risk for premature cardiovascular disease. The recognized cause is mutations of...

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Veröffentlicht in:	Journal of clinical lipidology 2016-05, Vol.10 (3), p.490-496
Hauptverfasser:	Chiou, Kuan-Rau, MD, Charng, Min-Ji, MD, PhD
Format:	Artikel
Sprache:	eng
Schlagworte:	Cardiovascular China - ethnology Chinese Ethnic Groups - genetics Familial hypercholesterolemia Genetics Humans Hyperlipoproteinemia Type II - diagnosis Hyperlipoproteinemia Type II - genetics Hyperlipoproteinemia Type II - metabolism Low-density lipoprotein receptor Molecular Diagnostic Techniques - methods Mutation Phenotype
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