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A combined LDL receptor/LDL receptor adaptor protein 1 mutation as the cause for severe familial hypercholesterolemia

Muhidien Soufi, Stephan Rust, Michael Walter, Juergen R. Schaefer

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Key concepts: Familial hypercholesterolemia, LDL receptor, Biology, PCSK9, Mutation, Apolipoprotein B, Internal medicine, Genetics

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A combined LDL receptor/LDL receptor adaptor protein 1 mutation as the cause for severe familial hypercholesterolemia — Research Paper | ScholarLens