Genetic Analysis in a Taiwanese Cohort of 750 Index Patients with Clinically Diagnosed Familial Hypercholesterolemia

Aim: Familial hypercholesterolemia (FH) is underdiagnosed in most countries. The genetic heterogeneity of FH requires an algorithm to efficiently integrate genetic testing into clinical practice. We aimed to report the spectrum of genetic mutations from patients with clinically diagnosed FH in Taiwa...

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Detalles Bibliográficos
Autores principales: Huang, Chin-Chou, Niu, Dau-Ming, Charng, Min-Ji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japan Atherosclerosis Society 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9135666/
https://www.ncbi.nlm.nih.gov/pubmed/33994402
http://dx.doi.org/10.5551/jat.62773

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9135666/
https://www.ncbi.nlm.nih.gov/pubmed/33994402
http://dx.doi.org/10.5551/jat.62773

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