{"id":"W2040612932","doi":"10.1038/ng1161","title":"Mutations in PCSK9 cause autosomal dominant hypercholesterolemia","year":2003,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Cholesterol and Lipid Metabolism","field":"Medicine","cited_by":3011,"is_retracted":false,"has_abstract":false,"ca_institutions":"Montreal Clinical Research Institute","funders":"Fondation de France; Institut National de la Santé et de la Recherche Médicale; Pfizer","keywords":"PCSK9; Kexin; Biology; Proprotein convertase; Apolipoprotein B; LDL receptor; Familial hypercholesterolemia; Lipoprotein; Locus (genetics); Subtilisin; Genetics; Endocrinology; Gene; Internal medicine; Cholesterol; Biochemistry; Medicine","routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false,"invisible_to_affiliation_only":false},"retraction":null,"screen":null}