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A double heterozygote for familial hypercholesterolaemia and familial defective apolipoprotein B-100

✍ Scribed by Taylor, A.; Bayly, G.; Patel, K.; Yarram, L.; Williams, M.; Hamilton-Shield, J.; Humphries, S. E.; Norbury, G.

Book ID
120038250
Publisher
Royal Society of Medicine Press
Year
2010
Tongue
English
Weight
114 KB
Volume
47
Category
Article
ISSN
0004-5632

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Phenotypic expression in double heterozy
Phenotypic expression in double heterozygotes for familial hypercholesterolemia and familial defective apolipoprotein B-100
✍ Pascale Benlian; Jean Luc de Gennes; FranΓ§ois Dairou; Brigitte Hermelin; Isabell πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 English βš– 554 KB

## Communicated by Michel Goossens Variability in the expression of monogenic lipid disorders may be observed in patients carrying the same DNA mutation, suggesting possible genetic or environmental interactions. Our objective was to investigate the genotype-phenotype relationships in two unrelate