Familial hypobetalipoproteinemia due to apolipoprotein B R463W mutation causes intestinal fat accumulation and low postprandial lipemia-Reference-Cited by-同舟云学术

Familial hypobetalipoproteinemia due to apolipoprotein B R463W mutation causes intestinal fat accumulation and low postprandial lipemia

Published:2009-09 Issue:1 Volume:206 Page:193-198
ISSN:0021-9150
Container-title:Atherosclerosis
language:en
Short-container-title:Atherosclerosis

Author:

Noto Davide,Cefalù Angelo B.,Cannizzaro Alessandra,Minà Mariangela,Fayer Francesca,Valenti Vincenza,Barbagallo Carlo M.,Tuttolomondo Antonino,Pinto Antonio,Sciumè Carmelo,Licata Giuseppe,Averna Maurizio

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference26 articles.

1. Lipid disorders and mutations in the APOB gene;Whitfield;Clin Chem,2004

2. Familial hypobetalipoproteinemia: genetics and metabolism;Schonfeld;Cell Mol Life Sci,2005

3. Absence of microsomal triglyceride transfer protein in individuals with abetalipoproteinemia;Wetterau;Science,1992

4. Microsomal triglyceride transfer protein, the abetalipoproteinemia gene product, mediates the secretion of apolipoprotein B-containing lipoproteins from heterologous cells;Leiper;J Biol Chem,1994

5. A novel nontruncating APOB gene mutation, R463W, causes familial hypobetalipoproteinemia;Burnett;J Biol Chem,2003

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