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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...
Enregistré dans:
| Publié dans: | J Investig Med High Impact Case Rep |
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| Auteurs principaux: | , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
SAGE Publications
2019
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| Sujets: | |
| Accès en ligne: | 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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