Normotriglyceridemic Abetalipoproteinemia in Infancy: An Isolated Apolipoprotein B-100 Deficiency
Author:
Affiliation:
1. From the Pediatric Clinic, Meijo Hospital, Naka-ku, Nagoya; Third Department of Internal Medicine, Faculty of Medicine, University of Tokyo; and Department of Laboratory Medicine, Faculty of Medicine, Gifu University, Gifu, Japan
Abstract
Publisher
American Academy of Pediatrics (AAP)
Subject
Pediatrics, Perinatology and Child Health
Link
https://publications.aap.org/pediatrics/article-pdf/75/3/541/957148/541.pdf
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Apolipoprotein Gene Mutations, Dyslipoproteinemia and Coronary Heart Disease;Human Genetics;1987
2. Parallel expression of the MB19 genetic polymorphism in apoprotein B-100 and apoprotein B-48. Evidence that both apoproteins are products of the same gene.;Journal of Biological Chemistry;1986-03
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