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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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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:J Investig Med High Impact Case Rep
Prif Awduron: Le, Ryan, Abbas, Minan, McIntyre, Adam D., Hegele, Robert A.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: SAGE Publications 2019
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC6755624/
https://ncbi.nlm.nih.gov/pubmed/31538826
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2324709619877050
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