Molecular Characterization of Familial Hypercholesterolemia in a North American Cohort
2019
Genotyping of 200 adults with clinical diagnosis of familial hypercholesterolemia from North America revealed that 40 percent of them had no disease-causing variants in LDLR, PCSK9 and APOB genes.
Keywords:
- Correction
- Source
- Cite
- Save
- Machine Reading By IdeaReader
68
References
7
Citations
NaN
KQI