Abstract
The DNA alteration in hereditary deficiency of apoA-I and C-III, variant 1, is one of the best characterized of all the dyslipoproteinemias. Since that discovery lipid metabolism has been examined in some detail in the two patients with this disorder. This report will review the clinical findings in the two patients and present results of studies on the physico-chemical properties and metabolism of their lipoproteins.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1986 Springer Science+Business Media New York
About this chapter
Cite this chapter
Norum, R.A., Forte, T.M., Alaupovic, P., Ginsberg, H.N. (1986). Clinical Syndrome and Lipid Metabolism in Hereditary Deficiency of Apolipoproteins A-I and C-III, Variant 1. In: Angel, A., Frohlich, J. (eds) Lipoprotein Deficiency Syndromes. Advances in Experimetal Medicine and Biology, vol 201. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-1262-8_13
Download citation
DOI: https://doi.org/10.1007/978-1-4684-1262-8_13
Publisher Name: Springer, Boston, MA
Print ISBN: 978-1-4684-1264-2
Online ISBN: 978-1-4684-1262-8
eBook Packages: Springer Book Archive