Familial hypercholesterolaemia: a study protocol for identification and investigation of potential causes and markers of subclinical coronary artery disease in the Faroe Islands

INTRODUCTION: Familial hypercholesterolaemia (FH) is the most common monogenic autosomal dominant genetic disorder and is associated with a high risk of premature atherosclerotic cardiovascular disease. The prevalence of FH has been reported to be particularly high in certain founder populations. Th...

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Detalles Bibliográficos
Autores principales: Borg, Sanna á, Nielsen, Michael Rene Skjelbo, Søgaard, Peter, Lundbye-Christensen, Søren, Jóanesarson, Jan, Zaremba, Tomas, Kollslíð, Rudi, Schmidt, Erik Berg, Joensen, Albert Marni, Bork, Christian Sørensen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Cardiovascular Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9006835/
https://www.ncbi.nlm.nih.gov/pubmed/35414540
http://dx.doi.org/10.1136/bmjopen-2021-050857

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9006835/
https://www.ncbi.nlm.nih.gov/pubmed/35414540
http://dx.doi.org/10.1136/bmjopen-2021-050857

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