Normal serum ApoB48 and red cells vitamin E concentrations after supplementation in a novel compound heterozygous case of abetalipoproteinemia
Author:
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine
Reference55 articles.
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1. A New Case of Abetalipoproteinemia Caused by Novel Compound Heterozygote Mutations in the <i>MTTP</i> Gene without Fat or Vitamin Malabsorption;Journal of Atherosclerosis and Thrombosis;2024
2. Missense mutation Q384K in the APOB gene affecting the large lipid transfer module of apoB reduces the secretion of apoB-100 in the liver without reducing the secretion of apoB-48 in the intestine;Journal of Clinical Lipidology;2023-11
3. Vitamin E: How much is enough, too much and why!;Free Radical Biology and Medicine;2021-12
4. Current Diagnosis and Management of Abetalipoproteinemia;Journal of Atherosclerosis and Thrombosis;2021-10-01
5. Normal plasma apoB48 despite the virtual absence of apoB100 in a compound heterozygote with novel mutations in the MTTP gene;Journal of Clinical Lipidology;2021-07
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