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Familial Hypercholesterolaemia

Familial hypercholesterolaemia (FH), defined as the heritable occurrence of severe hypercholesterolaemia with cholesterol deposits in tendons and premature heart disease, is caused by at least four genes in sterol and lipoprotein pathways and displays varying gene-dose effects. The genes are the low...

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Sparad:
Bibliografiska uppgifter
Huvudupphovsman: Marais, A David
Materialtyp: Artigo
Språk:Inglês
Publicerad: The Australian Association of Clinical Biochemists 2004
Ämnen:
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC1853359/
https://ncbi.nlm.nih.gov/pubmed/18516203
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