1998•Molecular and Cellular ProbesRequires access

Mutation analysis in familial hypercholesterolemia patients of different ancestries: identification of three novel LDLR gene mutations

Magda Callis, S Jansen, Rochelle Thiart, J. Nico P. de Villiers, Frederick J. Raal, Maritha J. Kotze

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Key concepts: Heteroduplex, Biology, Familial hypercholesterolemia, Genetics, LDL receptor, Exon, Single-strand conformation polymorphism, Mutation

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Mutation analysis in familial hypercholesterolemia patients of different ancestries: identification of three novel LDLR gene mutations — Research Paper | ScholarLens