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. The...

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Principais autores:	Peter Søgaard, Albert Marni Joensen, Søren Lundbye-Christensen, Erik Berg Schmidt, Jan Jóanesarson, Christian Sørensen Bork, Tomas Zaremba, Sanna á Borg, Michael Rene Skjelbo Nielsen, Rudi Kollslíð
פורמט:	Artigo
שפה:	Inglês
יצא לאור:	BMJ Publishing Group 2022-04-01
סדרה:	BMJ Open
גישה מקוונת:	https://bmjopen.bmj.com/content/12/4/e050857.full
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