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Large-scale deletions of the ABCA1 gene in patients with hypoalphalipoproteinemia
Copy-number variations (CNVs) have been studied in the context of familial hypercholesterolemia but have not yet been evaluated in patients with extreme levels of HDL cholesterol. We evaluated targeted, next-generation sequencing data from patients with very low levels of HDL cholesterol (i.e., hypo...
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| Gepubliceerd in: | J Lipid Res |
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| Hoofdauteurs: | , , , , , , , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
The American Society for Biochemistry and Molecular Biology
2018
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6071767/ https://ncbi.nlm.nih.gov/pubmed/29866657 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1194/jlr.P086280 |
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