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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Detalles Bibliográficos
Autores principales: Fairoozy, R. H., Futema, M., Vakili, R., Abbaszadegan, M. R., Hosseini, S., Aminzadeh, M., Zaeri, H., Mobini, M., Humphries, S. E., Sahebkar, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5719081/
https://www.ncbi.nlm.nih.gov/pubmed/29213121
http://dx.doi.org/10.1038/s41598-017-17181-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5719081/
https://www.ncbi.nlm.nih.gov/pubmed/29213121
http://dx.doi.org/10.1038/s41598-017-17181-9

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