The Genetic Spectrum of Familial Hypercholesterolemia (FH) in the Iranian Population

Familial hypercholesterolemia (FH) is an autosomal dominant disorder associated with premature cardiovascular disease (CVD). Mutations in the LDLR, APOB, and PCSK9 genes are known to cause FH. In this study, we analysed the genetic spectrum of the disease in subjects from the Iranian population with...

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Bibliografische gegevens
Gepubliceerd in:Sci Rep
Hoofdauteurs: Fairoozy, R. H., Futema, M., Vakili, R., Abbaszadegan, M. R., Hosseini, S., Aminzadeh, M., Zaeri, H., Mobini, M., Humphries, S. E., Sahebkar, A.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Nature Publishing Group UK 2017
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Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5719081/
https://ncbi.nlm.nih.gov/pubmed/29213121
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-017-17181-9
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