Familial Chylomicronemia Caused by a Novel Type of Mutation in the APOE-CI-CIV-CII Gene Cluster Encompassing Both the APOCII Gene and the First APOCIV Gene Mutation: APOCII-CIVNijmegen-Reference-Cited by-同舟云学术

Familial Chylomicronemia Caused by a Novel Type of Mutation in the APOE-CI-CIV-CII Gene Cluster Encompassing Both the APOCII Gene and the First APOCIV Gene Mutation: APOCII-CIVNijmegen

Published:2000-07 Issue:3 Volume:273 Page:1084-1087
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

de Graaf J.,Hoffer M.J.V.,Stuyt P.M.J.,Frants R.R.,Stalenhoef A.F.H.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference23 articles.

1. Hypertriglyceridemia Associated with Deficiency of Apolipoprotein C-II

2. THE FAMILIAL CHYLOMICRONEMIA SYNDROME

3. Premature Atherosclerosis in Patients with Familial Chylomicronemia Caused by Mutations in the Lipoprotein Lipase Gene

4. Apolipoprotein CIISt. Michael. Familial apolipoprotein CII deficiency associated with premature vascular disease.

5. The isolation and characterization of cDNA clones for human apolipoprotein CII.

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