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- W2966366886 abstract "Background and Aims: Familial Hypercholesterolemia (FH) is characterized by high LDL-cholesterol levels and high cardiovascular risk, being caused by mutations in LDLR, APOB, PCSK9, APOE, STAP1 or LDLRAP1 genes. The European Atherosclerosis Society (EAS) has recommended some criteria of clinical suspicion, but their sensitivity and efficiency have not been studied." @default.
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- W2966366886 date "2019-08-01" @default.
- W2966366886 modified "2023-10-16" @default.
- W2966366886 title "Sensitivity Of The Clinical Criteria For Suspected Familial Hypercholesterolemia In The Detection Of Diagnostic Mutations Of The Disease" @default.
- W2966366886 doi "https://doi.org/10.1016/j.atherosclerosis.2019.06.194" @default.
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