Article
Genotype/phenotype correlations in familial hypercholesterolaemia.
Current opinion in lipidology - 1 Aug 1998
Nicholls P, Young I S, Graham C A
Abstract excerpt
It is now possible to identify the specific gene defect in the majority of patients with familial hypercholesterolaemia. A potential benefit of this knowledge, in addition to helping with family screens, is to be able to predict the future clinical course. In order to do this, detailed genotype/p...
Topics
- Apolipoproteins B
- Genotype
- Humans
- Hyperlipoproteinemia Type II
- Mutation
- Phenotype
