Clinical syndrome and lipid metabolism in hereditary deficiency of apolipoproteins A-I and C-III, variant 1.
Clinical syndrome and lipid metabolism in hereditary deficiency of apolipoproteins A-I and C-III, variant 1.
复制标题
遗传性载脂蛋白 A-I 和 C-III 变体 1 缺乏症的临床综合征和脂质代谢。
DOI：
10.1007/978-1-4684-1262-8_13
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发表时间：
1986
影响因子：
--
通讯作者：
H. Ginsberg
中科院分区：
文献类型：
--
作者：
R. Norum;T. Forte;P. Alaupovic;H. Ginsberg
apoA-I和C-III遗传缺陷的DNA改变，变异1，是所有脂蛋白异常血症的最佳特征之一。自从这一发现以来，对这两名患者的脂质代谢进行了一些详细的检查。本文将回顾两例患者的临床表现，并介绍其脂蛋白的理化性质和代谢的研究结果。
The DNA alteration in hereditary deficiency of apoA-I and C-III, variant 1, is one of the best characterized of all the dyslipoproteinemias. Since that discovery lipid metabolism has been examined in some detail in the two patients with this disorder. This report will review the clinical findings in the two patients and present results of studies on the physico-chemical properties and metabolism of their lipoproteins.