Familial ligand-defective apolipoprotein B-100: detection, biochemical features and haplotype analysis of the R3531C mutation in the UK - Concepedia

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Familial ligand-defective apolipoprotein B-100: detection, biochemical features and haplotype analysis of the R3531C mutation in the UK

22

Citations

34

References

1997

Year

P R Wenham, Bryony G Henderson, Michael D. Penney, John Ashby, Peter Rae, Simon W. Walker

Atherosclerosis

Mendelian DisorderGenetic DisorderR3531c MutationGeneticsInherited Metabolic DiseaseHaplotype AnalysisHuman PolymorphismPathologyMolecular GeneticsVariant InterpretationMedicineBiochemical FeaturesClinical Genetics

References

	Year	Citations

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