Genetic Analysis of Iranian Patients with Familial Hypercholesterolemia

BACKGROUND: Familial hypercholesterolemia (FH) is a frequent autosomal dominant disorder of lipoprotein metabolism. This disorder is generally caused by mutations in low-density lipoprotein receptor (LDLR), apolipoprotein B 100 (APOB), and proprotein convertase subtilisin/kexin type 9 (PCSK9) genes....

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Detalles Bibliográficos
Autores principales: Ekrami, Mahdis, Torabi, Maryam, Ghafouri-Fard, Soudeh, Mowla, Javad, Soltani, Bahram Mohammad, Hashemi-Gorji, Feyzollah, Mohebbi, Zahra, Miryounesi, Mohammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pasteur Institute 2018
Materias:
Full Length
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5786657/
https://www.ncbi.nlm.nih.gov/pubmed/28734274
http://dx.doi.org/10.22034/ibj.22.2.117

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5786657/
https://www.ncbi.nlm.nih.gov/pubmed/28734274
http://dx.doi.org/10.22034/ibj.22.2.117

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