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The familial hyperchylomicronemia syndrome. New insights into underlying genetic defects.

作者信息

Santamarina-Fojo S, Brewer H B

机构信息

Molecular Disease Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Md. 20892.

出版信息

JAMA. 1991 Feb 20;265(7):904-8.

PMID:1992190
Abstract
摘要

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1
The familial hyperchylomicronemia syndrome. New insights into underlying genetic defects.
JAMA. 1991 Feb 20;265(7):904-8.
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[Chylomicronemia syndrome].[乳糜微粒血症综合征]
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Apolipoprotein C-II deficiency syndrome. Clinical features, lipoprotein characterization, lipase activity, and correction of hypertriglyceridemia after apolipoprotein C-II administration in two affected patients.载脂蛋白C-II缺乏综合征。两名患病患者的临床特征、脂蛋白特征、脂肪酶活性以及给予载脂蛋白C-II后高甘油三酯血症的纠正情况
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