Associated Papers
Genotype-phenotype studies of six novel LPL mutations in Chinese patients with hypertriglyceridemia.
Chan LY et al.
Human Mutation, 2002
Compound heterozygosity of Leu252Val and Leu252Arg causing lipoprotein lipase deficiency in a chinese patient with hypertriglyceridemia.
Chan L et al.
European Journal of Clinical Investigation, 2000
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