Knockout of the abetalipoproteinemia gene in mice: Reduced lipoprotein secretion in heterozygotes and embryonic lethality in homozygotes
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference39 articles.
1. Abetalipoproteinemia
2. Absorption, lipoprotein transport, and regulation of plasma concentrations of vitamin E in humans.
3. Absence of Microsomal Triglyceride Transfer Protein in Individuals with Abetalipoproteinemia
4. Abetalipoproteinemia is caused by defects of the gene encoding the 97 kDa subunit of a microsomal triglyceride transfer protein
5. Cloning and gene defects in microsomal triglyceride transfer protein associated with abetalipoproteinaemia
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