A case of apolipoprotein A-I deficiency due to carboxyl-terminal truncation
Author:
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine,Nutrition and Dietetics,Endocrinology, Diabetes and Metabolism,Internal Medicine
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1. A novel homozygous frameshift mutation in the APOA1 gene associated with marked high-density lipoprotein deficiency;Journal of Clinical Lipidology;2022-07
2. Apolipoprotein genetic variants and hereditary amyloidosis;Current Opinion in Lipidology;2020-12-31
3. The brave new world of genetic testing in the management of the dyslipidaemias;Current Opinion in Cardiology;2020-05
4. Inborn errors of apolipoprotein A-I metabolism;Current Opinion in Lipidology;2020-04
5. Rare dyslipidaemias, from phenotype to genotype to management: a European Atherosclerosis Society task force consensus statement;The Lancet Diabetes & Endocrinology;2020-01
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