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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Publicado en:Sci Rep
Main Authors: Fairoozy, R. H., Futema, M., Vakili, R., Abbaszadegan, M. R., Hosseini, S., Aminzadeh, M., Zaeri, H., Mobini, M., Humphries, S. E., Sahebkar, A.
Formato: Artigo
Idioma:Inglês
Publicado: Nature Publishing Group UK 2017
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Article
Acceso en liña: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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