Genomewide scan for familial combined hyperlipidemia genes in finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels.

Familial combined hyperlipidemia (FCHL) is a common dyslipidemia predisposing to premature coronary heart disease (CHD). The disease is characterized by increased levels of serum total cholesterol (TC), triglycerides (TGs), or both. We recently localized the first locus for FCHL, on chromosome 1q21-...

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Autors principals: Pajukanta, P, Terwilliger, J D, Perola, M, Hiekkalinna, T, Nuotio, I, Ellonen, P, Parkkonen, M, Hartiala, J, Ylitalo, K, Pihlajamäki, J, Porkka, K, Laakso, M, Viikari, J, Ehnholm, C, Taskinen, M R, Peltonen, L
Format: Artigo
Idioma:Inglês
Publicat: 1999
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377884/
https://ncbi.nlm.nih.gov/pubmed/10205279
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