Clinical characterization and mutation spectrum of German patients with familial hypercholesterolemia. [electronic resource]
Producer: 20171221Description: 88-93 p. digitalISSN:- 1879-1484
- Adult
- Alleles
- Apolipoproteins B -- genetics
- Cholesterol, LDL -- blood
- DNA Mutational Analysis
- Exons
- Female
- Genetic Association Studies
- Genetic Variation
- Germany
- Humans
- Hyperlipoproteinemia Type II -- blood
- Male
- Middle Aged
- Mutation
- Mutation, Missense
- Phenotype
- Proprotein Convertase 9 -- genetics
- Proprotein Convertases -- genetics
- ROC Curve
- Receptors, LDL -- genetics
- Serine Endopeptidases -- genetics
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Publication Type: Journal Article
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