Familial Hypercholesterolemia: Real-World Data of 1236 Patients Attending a Czech Lipid Clinic. A Retrospective Analysis of Experience in More than 50 years. Part I: Genetics and Biochemical Parameters

Introduction: The cause of familial hypercholesterolemia (FH) is defect in LDL receptor or familial defect of apolipoprotein B-100 (FDB) or, rarely, defect in proprotein convertase subtilisin/kexin type 9. Identification and treatment of patients with FH improves their prognosis. Our data represent...

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Detalles Bibliográficos
Autores principales: Todorovova, Veronika, Altschmiedova, Tereza, Vrablik, Michal, Ceska, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8918685/
https://www.ncbi.nlm.nih.gov/pubmed/35295947
http://dx.doi.org/10.3389/fgene.2022.849008

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8918685/
https://www.ncbi.nlm.nih.gov/pubmed/35295947
http://dx.doi.org/10.3389/fgene.2022.849008

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