Hypobetalipoproteinemia
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Publisher
Elsevier
Reference127 articles.
1. Disorders of the biogenesis and secretion of lipoproteins containing the B apolipoproteins;Kane,2001
2. Monogenic hypocholesterolaemic lipid disorders and apolipoprotein B metabolism;Hooper;Crit. Rev. Clin. Lab. Sci.,2005
3. Familial hypobetalipoproteinemia: genetics and metabolism;Schonfeld;Cell. Mol. Life Sci.,2005
4. Complexity in the secretory pathway: the assembly and secretion of apolipoprotein B-containing lipoproteins;Fisher;J. Biol. Chem.,2002
5. The many intersecting pathways underlying apolipoprotein B secretion and degradation;Brodsky;Trends Endocrinol. Metab.,2008
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1. Primary hypocholesterolemia is associated with an increased risk of hepatic complications in the general population;Journal of Hepatology;2024-02
2. Hipobetalipoproteinemia familiar ApoB específica en una paciente con hiperplasia suprarrenal congénita no clásica;Clínica e Investigación en Arteriosclerosis;2024-01
3. Inborn Errors of Metabolism with Ataxia: Current and Future Treatment Options;Cells;2023-09-19
4. Interest of minigene splicing reporter assay in familial hypobetalipoproteinemia genetic diagnosis: the example of the missense mutation APOB c.1468C>T;Clinical Chemistry and Laboratory Medicine (CCLM);2023-06-14
5. Non-alcoholic fatty liver disease in a pediatric patient with heterozygous familial hypobetalipoproteinemia due to a novel APOB variant: a case report and systematic literature review;Frontiers in Medicine;2023-06-13
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