[Clinical manifestations and genetic analysis of two patients with familial hypercholesterolemia caused by complex heterozygous variants].
Patients 1 and 2 in this study were patients with complex heterozygous variant FH, and their genotypic differences may be related to the differences in clinical serum LDL-C levels and the efficacy of hypolipidemic agents.
Authors
- Xifu Wang (ORCID: https://orcid.org/0000-0001-5225-8140)
- Xiangyang Li (ORCID: https://orcid.org/0009-0001-3360-7381)
- Xiang Lian (ORCID: https://orcid.org/0000-0001-7681-3807)
- Chunying Tian
- Zixi Liu (ORCID: https://orcid.org/0000-0002-7709-1487)
- Kexin Wang (ORCID: https://orcid.org/0000-0002-6170-4744)
Institutions
- Beijing Anzhen Hospital (CN)
Publication Details
- Journal
- PubMed
- Published
- 2025-02-10
- DOI
- https://doi.org/10.3760/cma.j.cn511374-20241026-00562
- Primary Topic
- Lipoproteins and Cardiovascular Health
- Type
- article
- Field-Weighted Citation Impact
- 0.00