Genetic evidence from 7 families that the apolipoprotein B gene is not involved in familial combined hyperlipidemia

Familial combined hyperlipidemia (FCHL) is the most common genetic form of hyperlipidemia in which affected individuals manifest multiple lipoprotein phenotypes. Although the molecular defect is still unknown, several kinetic studies have demonstrated increased turnover rates of apolipoprotein B (ap...

Ausführliche Beschreibung