Severe Combined Dyslipidemia With a Complex Genetic Basis

Background. Familial dysbetalipoproteinemia (also known as type 3 hyperlipoproteinemia) is typically associated with homozygosity for the apolipoprotein E2 isoform, but also sometimes with dominant rare missense variants in the APOE gene. Patients present with roughly equimolar elevations of cholest...

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Detalles Bibliográficos
Autores principales: Le, Ryan, Abbas, Minan, McIntyre, Adam D., Hegele, Robert A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6755624/
https://www.ncbi.nlm.nih.gov/pubmed/31538826
http://dx.doi.org/10.1177/2324709619877050

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6755624/
https://www.ncbi.nlm.nih.gov/pubmed/31538826
http://dx.doi.org/10.1177/2324709619877050

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