Mutational Spectrum of LDLR and PCSK9 Genes Identified in Iranian Patients With Premature Coronary Artery Disease and Familial Hypercholesterolemia

Familial hypercholesterolemia (FH) is a common, yet underdiagnosed, genetic disorder characterized by lifelong elevated low-density lipoprotein cholesterol levels, which can increase the risk of early-onset coronary artery disease (CAD). In the present study, we screened the nucleotide variations of...

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Detalles Bibliográficos
Autores principales: Moradi, Arman, Maleki, Majid, Ghaemmaghami, Zahra, Khajali, Zahra, Noohi, Feridoun, Moghadam, Maryam Hosseini, Kalyinia, Samira, Mowla, Seyed Javad, Seidah, Nabil G., Malakootian, Mahshid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7959244/
https://www.ncbi.nlm.nih.gov/pubmed/33732287
http://dx.doi.org/10.3389/fgene.2021.625959

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7959244/
https://www.ncbi.nlm.nih.gov/pubmed/33732287
http://dx.doi.org/10.3389/fgene.2021.625959

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