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January 1, 1995Journal of Internal Medicine

Heterozygous familial hypercholesterolaemia: the influence of the mutation type of the low‐density‐lipoprotein receptor gene and PvuII polymorphism of the normal allele on serum lipid levels and response to lovastatin treatment

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Authors

AVA. F. VUORIOJOJukka-Pekka OjalaSSSeppo SarnaUniversity College London Hospitals NHS Foundation Trust

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VUORIO et al. (1995) studied this question.

synapsesocial.com/papers/6a9a50f2b5946d86254e2ad3https://doi.org/10.1111/j.1365-2796.1995.tb01138.x
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Also Consider

Synapse has enriched one closely related paper. Consider it for comparative context:

  1. 1Finnish type of low density lipoprotein receptor gene mutation (FH-Helsinki) deletes exons encoding the carboxy-terminal part of the receptor and creates an internalization-defective phenotype.1989 · 103 citations