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Usefulness of the genetic risk score to identify phenocopies in families with familial hypercholesterolemia?

Archive ouverte | Ghaleb, Youmna | CCSD

International audience. Familial hypercholesterolemia (FH) is caused by mutations in LDLR (low-density lipoprotein receptor), APOB (apolipoprotein B), PCSK9 (proprotein convertase subtilisin/kexin type 9), or APOE (...

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Archive ouverte | Ayoub, Carine | CCSD

International audience. Familial hypobetalipoproteinemia (FHBL) is a codominant genetic disorder characterized by reduced plasma levels of low-density lipoprotein cholesterol and apolipoprotein B. To our knowl-edge,...

Improved plasma cholesterol efflux capacity from human macrophages in patients with hyperalphalipoproteinemia

Archive ouverte | El Khoury, Petra | CCSD

International audience

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