Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes

We and others have recently identified mutations in the ABCA1 gene as the underlying cause of Tangier disease (TD) and of a dominantly inherited form of familial hypoalphalipoproteinemia (FHA) associated with reduced cholesterol efflux. We have now identified 13 ABCA1 mutations in 11 families (five...

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Autors principals: Clee, Susanne M., Kastelein, John J.P., van Dam, Marjel, Marcil, Michel, Roomp, Kirsten, Zwarts, Karin Y., Collins, Jennifer A., Roelants, Roosje, Tamasawa, Naoki, Stulc, Tomás, Suda, Toshihiro, Ceska, Richard, Boucher, Betsie, Rondeau, Colette, DeSouich, Christele, Brooks-Wilson, Angela, Molhuizen, Henri O.F., Frohlich, Jiri, Genest, Jacques, Hayden, Michael R.
Format: Artigo
Idioma:Inglês
Publicat: American Society for Clinical Investigation 2000
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC381437/
https://ncbi.nlm.nih.gov/pubmed/11086027
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