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6th Hellenic Congress in Athens, of the Hellenic Atherosclerosis Society, on the 04-06 December 2014 Novel Pharmacologic Treatments of Familial Hypercholesterolaemia

Familial hypercholesterolaemia (FH) is the most common inherited monogenic lipid disorder. It is caused by mutations of genes related to low density lipoprotein (LDL) receptors, apolipoprotein B or proprotein convertase subtilisin/kexin type 9 (PCSK9). Homozygous FH (HoFH; 1/400,000 births) is treat...

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Xehetasun bibliografikoak
Argitaratua izan da:Open Cardiovasc Med J
Egile nagusia: Athyros, VG
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Bentham Open 2015
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4645966/
https://ncbi.nlm.nih.gov/pubmed/26664657
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2174/1874192401509010073
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