Apolipoprotein B-52 mutation associated with hypobetalipoproteinemia is compatible with a misaligned pairing deletion mechanism
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Endocrinology,Biochemistry
Reference48 articles.
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3. ApoB-75, a truncation of apolipoprotein-B associated with familial hypobetalipo-proteinemia: genetic and kinetic studies;Krul;J. Lipid Res.,1992
4. Two distinct truncated apolipoprotein B species in a kindred with hypobetalipoproteinemia;Krul;Arteriosclerosis.,1989
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2. Monogenic Hypocholesterolaemic Lipid Disorders and Apolipoprotein B Metabolism;Critical Reviews in Clinical Laboratory Sciences;2005-01
3. Fatty liver in familial hypobetalipoproteinemia: triglyceride assembly into VLDL particles is affected by the extent of hepatic steatosis;Journal of Lipid Research;2003-03
4. A study of fatty liver disease and plasma lipoproteins in a kindred with familial hypobetalipoproteinemia due to a novel truncated form of apolipoprotein B (APO B-54.5);Journal of Hepatology;2000-09
5. Diabetes mellitus in a new kindred with familial hypobetalipoproteinemia and an apolipoprotein B truncation (apoB-55);Atherosclerosis;1998-02
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