Familial defective apolipoprotein B-100: a tale of twin mutations

被引：4

作者：

Andersen, Lars H. ^{[1
]}

Andersen, Rolf L. ^{[1
]}

Miserez, Andre R. ^{[2
,3
]}

机构：

[1] Lancaster Gen Hlth Penn Med, Res Inst, Lancaster, PA 17602 USA

[2] Univ Basel, Basel, Switzerland

[3] Diagene Labs Inc, Res Inst, Reinach, Switzerland

来源：

JOURNAL OF CLINICAL LIPIDOLOGY | 2016年 / 10卷 / 04期

关键词：

SOUTH EUROPEAN POPULATION; LOW-DENSITY LIPOPROTEINS; RECEPTOR GENE-MUTATIONS; APO-B GENE; HYPERCHOLESTEROLEMIA PATIENTS; R3500Q MUTATION; MOLECULAR-BASIS; PHENOTYPE; IDENTIFICATION; BINDING;

D O I：

10.1016/j.jacl.2016.04.007

中图分类号：

R9 [药学];

学科分类号：

1007 ;

摘要：

引用

页码：1050 / 1051

页数：2

共 27 条

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