CASCADE screening and registry of familial hypercholesterolemia in Iran: Rationale and design

BACKGROUND: Familial hypercholesterolemia (FH) is one of the most common genetic disorders, which leads to premature coronary artery disease (CAD). It has been suggested that heterozygous FH affects around 1:250 to 1:500 in the general population or even more than this, and homozygous FH affects 1:1...

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Dades bibliogràfiques
Publicat a:ARYA Atheroscler
Autors principals: Vaseghi, Golnaz, Arabi, Sina, Haghjooy-Javanmard, Shaghayegh, Sabri, Mohammadreza, Sadeghi, Masoumeh, Khosravi, Alireza, Zarfeshani, Sonia, Sarrafzadegan, Nizal
Format: Artigo
Idioma:Inglês
Publicat: Isfahan Cardiovascular Research Center, Isfahan University of Medical Sciences 2019
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Original Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6679656/
https://ncbi.nlm.nih.gov/pubmed/31440286
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.22122/arya.v15i2.1899
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