Editorial comment: Frequent detection of familial hypercholesterolemia mutations in familial combined hyperlipidemia

Ítems similars

• Mutation detection in Chinese patients with familial hypercholesterolemia
  per: Du, Ran, et al.
  Publicat: (2016)
• DIFFERENTIAL IMPACT OF FAMILIAL HYPERCHOLESTEROLEMIA AND COMBINED HYPERLIPIDEMIA ON VASCULAR WALL AND NETWORK REMODELING IN MICE
  per: Stapleton, Phoebe A., et al.
  Publicat: (2010)
• Hyperlipidemia in Coronary Heart Disease II. GENETIC ANALYSIS OF LIPID LEVELS IN 176 FAMILIES AND DELINEATION OF A NEW INHERITED DISORDER, COMBINED HYPERLIPIDEMIA
  per: Goldstein, Joseph L., et al.
  Publicat: (1973)
• A mutation in the promoter of the lipoprotein lipase (LPL) gene in a patient with familial combined hyperlipidemia and low LPL activity.
  per: Yang, W S, et al.
  Publicat: (1995)
• Linkage and association analyses identify a candidate region for apoB level on chromosome 4q32.3 in FCHL families
  per: Wijsman, Ellen M., et al.
  Publicat: (2010)